Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: Muscle biopsy and autopsy findings, biochemical and molecular genetic studies
Neuromuscular Disorders2010Vol. 20(12), pp. 783–790
Citations Over TimeTop 13% of 2010 papers
A.L. Taratuto, Hasan O. Akman, M. Saccoliti, Miguel A. Riudavets, Naomí Arakaki, L. Mesa, Gustavo Sevlever, Hans H. Goebel, S. DiMauro
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