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Neuromuscular Disorders : NMD|December 7, 2002
The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C geneM Chaouch, Y Allal, A De Sandre-Giovannoli, et al.
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Showing results (51-60 of 51) with videos related to

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Pageof 6
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Neuromuscular Disorders : NMD|December 7, 2002
The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C geneM Chaouch, Y Allal, A De Sandre-Giovannoli, et al.
Pageof 6