Facioscapulohumeral dystrophy: A distinct regional myopathy with a novel molecular pathogenesis-Reference-Cited by-同舟云学术

Facioscapulohumeral dystrophy: A distinct regional myopathy with a novel molecular pathogenesis

Published:1998-03 Issue:3 Volume:43 Page:279-282
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Tawil Rabi,Figlewicz Denise A.,Griggs Robert C.,Weiffenbach Barbara,

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference32 articles.

1. Facioscapulohumeral disease. Leiden, The Netherlands, University of Leiden, 1982. Thesis

2. Facioscapulohumeral muscular dystrophy. In, eds. The molecular and genetic basis of neurological disease. Boston: Butterworth-Heinemann, 1997: 931-938.

3. On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy

4. RETINAL VASCULAR ABNORMALITIES IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY

5. Facioscapulohumeral muscular dystrophy: Evidence for selective, genetic electrophysiologic cardiac involvement

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