Muscular Dystrophy- Facioscapulohumeral Dystrophy - A Rare Autosomal Dominant Disorder
Author:
Publisher
Akshantala Enterprises Private Limited
Subject
General Medicine
Link
https://www.jemds.com/data_pdf/rajesh%20kumar-may-18-CR-C.pdf
Reference12 articles.
1. Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample;Mostacciuolo;Clin Genet,2009
2. 3 kb element;Gabriëls;Gene,1999
3. [3] Richards M, Coppée F, Thomas N, et al. Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? Hum Genet 2012;131(3):325-40.
4. Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHD;Upadhyaya;J Med Genet,1997
5. 171st ENMC International Workshop: Standards of care and management of facioscapulohumeral muscular dystrophy;Tawil;Neuromuscul Disord,2010
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