Pediatric Neurology Briefs
Published 2003 | Version v1.0.0
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Limb-Girdle Muscular Dystrophies

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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.

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PNB-17-39-a

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Created
2003
When the item was originally created.