Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation (Q78190267)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

title

Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Maria Laura Manca

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Michelangelo Mancuso

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

author name string

A Tessa

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

M Renna

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

L Murri

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

publication date

1 July 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

volume

56

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

page(s)

51-58

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

Subcellular fractionation of dystrophin to the triads of skeletal muscle

12 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Prevalence and incidence of Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Prognostic factors in mild dystrophinopathies

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Early diagnosis of Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotype

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

The prevalence of inherited neuromuscular disease in Northern Ireland

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Prevalence and incidence of muscular dystrophy in Alberta, Canada

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Population data on benign and severe forms of X-linked muscular dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Prevalent cardiac involvement in dystrophin Becker type mutation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Clinical features and classification of the muscular dystrophies

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

The frequency of patients with dystrophin abnormalities in a limb-girdle patient population

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560107.X

7 January 2021

10.1034/J.1399-0004.1999.560107.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10466417%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

1 reference