Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: Muscle biopsy and autopsy findings, biochemical and molecular genetic studies
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S. Dimauro | G. Sevlever | A. Taratuto | H. Akman | M. Riudavets | N. Arakaki | M. Saccoliti | H. Goebel | L. Mesa | N. Arakaki | L. Mesa