N-Glycolylneuraminic acid deficiency worsens cardiac and skeletal muscle pathophysiology in α-sarcoglycan-deficient mice

Roughly 3 million years ago, an inactivating deletion occurred in CMAH, the human gene encoding CMP-Neu5Ac (cytidine-5′-monophospho-N-acetylneuraminic acid) hydroxylase (Chou HH, Takematsu H, Diaz S, Iber J, Nickerson E, Wright KL, Muchmore EA, Nelson DL, Warren ST, Varki A. 1998. A mutation in huma...

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Bibliografische gegevens
Hoofdauteurs: Martin, Paul T, Camboni, Marybeth, Xu, Rui, Golden, Bethannie, Chandrasekharan, Kumaran, Wang, Chiou-Miin, Varki, Ajit, Janssen, Paul M L
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2013
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Original Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3671774/
https://ncbi.nlm.nih.gov/pubmed/23514716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/glycob/cwt020
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