Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland (Q34627289)

3 August 2017

title

Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland (English)

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3 August 2017

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Corrado Angelini

6

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Leena Peltonen-Palotie

7

object named as

Leena Peltonen

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3 August 2017

Tiina Suominen

1

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3 August 2017

Linda L Bachinski

2

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3 August 2017

Satu Auvinen

3

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3 August 2017

Peter Hackman

4

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3 August 2017

Keith A Baggerly

5

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3 August 2017

Ralf Krahe

8

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3 August 2017

Bjarne Udd

9

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3 August 2017

publication date

2 March 2011

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European Journal of Human Genetics

3 August 2017

number of pages

7

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published in

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3 August 2017

volume

19

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3 August 2017

issue

7

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3 August 2017

page(s)

776-782

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https://scigraph.springernature.com/pub.10.1038/ejhg.2011.23

3 August 2017

exact match

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cites work

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Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia

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High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany

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Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions

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12 December 2020

Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis

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Ethnic distribution of myotonic dystrophy gene

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Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations

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Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member

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Origin and Diffusion of the Myotonic Dystrophy Gene in the Saguenay Region (Quebec)

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Identifiers

DOI

10.1038/EJHG.2011.23

1 reference

3 August 2017

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3 August 2017

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