Limb-Girdle Muscular Dystrophies
Abstract
The phenotype in limb-girdle muscular dystrophy (LGMD) type 21 was defined by mutation analysis, protein studies, and respiratory and cardiac involvement studied in 16 patients from 14 families with fukutin-related protein (FKRP) gene mutations and LGMD, at the Institute of Human Genetics, University Newcastle upon Tyne, UK.
DOI: https://doi.org/10.15844/pedneurbriefs-17-5-6 | Journal eISSN: 2166-6482
Language: English
Page range: 39 - 39
Published on: May 1, 2003
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2003 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.