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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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2003-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | 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. |
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| Item Description: | 1043-3155 2166-6482 10.15844/pedneurbriefs-17-5-6 |