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Article

Prenatal muscle development in a mouse model for the secondary dystroglycanopathies.

Skeletal muscle - 1 Jan 2016

Kim Jihee, Hopkinson Mark, Kavishwar Manoli, Fernandez-Fuente Marta, Brown Susan Carol

Abstract excerpt

BACKGROUND: The defective glycosylation of α-dystroglycan is associated with a group of muscular dystrophies that are collectively referred to as the secondary dystroglycanopathies. Mutations in the gene encoding fukutin-related protein (FKRP) are one of the most common causes of secondary dystroglycanopathy in the UK and are associated with a wide spectrum of disease. Whilst central nervous system involvement...

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Source

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Identifiers

PMID: 26900448
DOI: 10.1186/s13395-016-0073-y
PMCID: PMC4759920

Genes

FKRP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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