Diagnostic clinique et moléculaire de la myopathie facioscapulo-humérale de type 1 (FSHD1) en 2012-Reference-Cited by-同舟云学术

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Diagnostic clinique et moléculaire de la myopathie facioscapulo-humérale de type 1 (FSHD1) en 2012

Published:2013-08 Issue:8-9 Volume:169 Page:573-582
ISSN:0035-3787
Container-title:Revue Neurologique
language:fr
Short-container-title:Revue Neurologique

Author:

Salort-Campana E.,Nguyen K.,Lévy N.,Pouget J.,Attarian S.

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference103 articles.

1. Recommendations for the management of facioscapulohumeral muscular dystrophy in 2011;Attarian;Rev Neurol,2012

2. Beevor's sign and facioscapulohumeral dystrophy;Awerbuch;Arch Neurol,1990

3. The FSHD-linkedlocus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter;Bakker;Muscle Nerve,1995

4. Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases;Bakker;J Med Genet,1996

5. Phenotypic clustering of lamin A/C mutations in neuromuscular patients;Benedetti;Neurology,2007

Cited by 1 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. Facioscapulohumeral Muscular Dystrophy;Comprehensive Physiology;2017-09-12

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