Limb-Girdle Muscular Dystrophies
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, Universit...
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| Médium: | Článek |
| Jazyk: | English |
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Pediatric Neurology Briefs Publishers
2003-05-01
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| Edice: | Pediatric Neurology Briefs |
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| On-line přístup: | https://www.pediatricneurologybriefs.com/articles/1514 |