Genetic heterogeneity of autosomal recessive limbgirdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus

Author:

Allamand V.,Broux O.,Bourg N.,Richard I.,Tischfield J.A.,Hodes M.E.,Conneally P.M.,Fardeau M.,Jackson C.E.,Beckmann J.S.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Cited by 32 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The Limb-Girdle Muscular Dystrophies;CONTINUUM: Lifelong Learning in Neurology;2022-12

2. Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations;International Journal of Molecular Sciences;2019-09-13

3. Limb girdle muscular dystrophies: clinical-genetical diagnostic update and prospects for therapy;Expert Opinion on Orphan Drugs;2017-08-23

4. Natural history of LGMD2A for delineating outcome measures in clinical trials;Annals of Clinical and Translational Neurology;2016-03-04

5. Where do we stand in trial readiness for autosomal recessive limb girdle muscular dystrophies?;Neuromuscular Disorders;2016-02

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