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...
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Pediatric Neurology Briefs Publishers
2003-05-01
|
| Schriftenreihe: | Pediatric Neurology Briefs |
| Schlagworte: | |
| Online-Zugang: | https://www.pediatricneurologybriefs.com/articles/1514 |
| Tags: |
Keine Tags, Fügen Sie das erste Tag hinzu!
|