Familial Parkinson's disease: a clinical genetic analysis (Q70997094)

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15 October 2019

title

Familial Parkinson's disease: a clinical genetic analysis (English)

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15 October 2019

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V Bonifati

1

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15 October 2019

E Fabrizio

2

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15 October 2019

N Vanacore

3

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15 October 2019

M De Mari

4

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15 October 2019

G Meco

5

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15 October 2019

publication date

1 November 1995

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Canadian Journal of Neurological Sciences

15 October 2019

language of work or name

English

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published in

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15 October 2019

volume

22

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15 October 2019

issue

4

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15 October 2019

page(s)

272-279

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Parkinson's disease: a test of the multifactorial etiologic hypothesis

15 October 2019

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Paternal preponderance in familial Parkinson's disease

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

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A clinical and genetic study of familial Parkinson's disease

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

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Anticipation of onset age in familial Parkinson's disease

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A clinical genetic study of Parkinson's disease: evidence for dominant transmission

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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

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Isolated tremor and disruption of the nigrostriatal dopaminergic system: An 18F-dopa PET study

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Molecular genetics of Huntington's disease

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The use of life tables and survival analysis in testing genetic hypotheses, with an application to Alzheimer's disease

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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

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7 January 2021

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7 January 2021

A large kindred with autosomal dominant Parkinson's disease

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7 January 2021

Parkinson's disease. A genetic study

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7 January 2021

10.1017/S0317167100039469

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8599769%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

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