A natural history study in Limb Girdle Muscular Dystrophy 2I : magnetic resonance imaging, spectroscopy and physical outcome measures

Limb Girdle Muscular Dystrophy 2I (LGMD2I) is caused by mutations in the fukutin related protein gene (FKRP). It is an important and frequent cause of LGMD, particularly in Northern Europe, and can range from a severe muscular dystrophy in childhood, very similar to Duchenne muscular dystrophy, to a...

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Bibliographic Details
Main Author: Willis, Tracey Anne
Published: University of Newcastle upon Tyne 2012
Subjects:
Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570325