Genetics of Facioscapulohumeral Muscular Dystrophy
Abstract
More than 500 subjects from 41 families with dominantly inherited facioscapulohumeral muscular dystrophy (FSHD) were studied at the Royal Hospital for Sick Children, St. Michael’s Hill, Bristol and the University of Wales College of Medicine, Heath Park, Cardiff, Wales.
DOI: https://doi.org/10.15844/pedneurbriefs-5-11-1 | Journal eISSN: 2166-6482
Language: English
Page range: 81 - 82
Published on: Nov 1, 1991
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 1991 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.