Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study-Reference-Cited by-同舟云学术

Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study

Published:2018-10-16 Issue:5 Volume:84 Page:627-637
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Goselink Rianne J.M.¹,Schreuder Tim H.A.¹,van Alfen Nens¹,de Groot Imelda J.M.²,Jansen Merel²,Lemmers Richard J.L.F.³,van der Vliet Patrick J.³,van der Stoep Nienke⁴,Theelen Thomas⁵,Voermans Nicol C.¹,van der Maarel Silvère M.³,van Engelen Baziel G.M.¹,Erasmus Corrie E.¹

Affiliation:

1. Department of Neurology, Donders Centre for NeuroscienceRadboud University Medical Centre Nijmegen The Netherlands

2. Department of Rehabilitation, Donders Centre for NeuroscienceRadboud University Medical Centre Nijmegen The Netherlands

3. Department of Human GeneticsLeiden University Medical Centre Leiden The Netherlands

4. Department of Clinical GeneticsLeiden University Medical Centre Leiden The Netherlands

5. Department of OphthalmologyRadboud University Medical Centre Nijmegen The Netherlands

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25326

Reference59 articles.

1. Population-based incidence and prevalence of facioscapulohumeral dystrophy

2. Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere

3. Facioscapulohumeral dystrophy: the path to consensus on pathophysiology

4. Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy

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