Molecular basis of AMP deaminase deficiency in skeletal muscle.

AMP deaminase (AMPD; EC 3.5.4.6) is encoded by a multigene family in mammals. The AMPD1 gene is expressed at high levels in skeletal muscle, where this enzyme is thought to play an important role in energy metabolism. Deficiency of AMPD activity in skeletal muscle is associated with symptoms of a me...

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Bibliographic Details
Main Authors: Morisaki, T, Gross, M, Morisaki, H, Pongratz, D, Zöllner, N, Holmes, E W
Format: Artigo
Language:Inglês
Published: 1992
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC49520/
https://ncbi.nlm.nih.gov/pubmed/1631143
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