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Article

[Defective O-mannosyl glycosylation causes congenital muscular dystrophies].

Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme - 1 Nov 2004

Manya Hiroshi, Endo Tamao

Abstract excerpt

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Share to Abnormalities, Multiple
Share to Dystroglycans
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15553000

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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[Defective O-mannosyl glycosylation causes congenital muscular dystrophies].PMID 15553000Read ↗

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The o-mannosylation pathway: glycosyltransferases and proteins implicated in congenital muscular dystrophy.Semantic proximity Read ↗

[Finding of O-mannosyl glycan in mammals and congenital muscular dystrophies due to glycosylation defects].Semantic proximity Read ↗

Structure, function and pathology of O-mannosyl glycans.Semantic proximity Read ↗

Protein glycosylation in disease: new insights into the congenital muscular dystrophies.Semantic proximity Read ↗

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Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypes.Semantic proximity Read ↗

[Congenital disorders of glycosylation].Semantic proximity Read ↗

Mammalian O-mannosylation: unsolved questions of structure/function.Semantic proximity Read ↗

Mannosyl-oligosaccharide glucosidase - congenital disorder of glycosylation: A patient with novel variants.Semantic proximity Read ↗

[Congenital disorder of glycosylation type Ia (CDG Ia) - underdiagnosed entity?].Semantic proximity Read ↗

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