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Congenital Muscular Dystrophies Involving the O-Mannose Pathway

A number of forms of congenital muscular dystrophy (CMD) have been identified that involve defects in the glycosylation of dystroglycan with O-mannosyl-linked glycans. There are at least six genes that can affect this type of glycosylation, and defects in these genes give rise to disorders that have...

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Bibliografske podrobnosti
Glavni avtor: Martin, Paul T.
Format: Artigo
Jezik:Inglês
Izdano: 2007
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2855644/
https://ncbi.nlm.nih.gov/pubmed/17584082
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