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Article

Minimal Consequences of CMAH and DBA/2 Backgrounds on a FKRP Deficient Model.

Journal of neuromuscular diseases - 1 Jan 2021

Vaubourg Camille, Gicquel Evelyne, Richard Isabelle, Lostal William, Bellec Jessica

Abstract excerpt

BACKGROUND: Muscular dystrophies (MD) are a large group of genetic diseases characterized by a progressive loss of muscle. The Latent TGFβ Binding Protein 4 (LTBP4) in the DBA/2 background and the Cytidine Monophosphate-sialic Acid Hydroxylase (CMAH) proteins were previously identified as genetic modifiers in severe MD. OBJECTIVE: We investigated whether these modifiers could also influence a mild phenotype such...

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Share to Disease Models, Animal
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Muscular Dystrophies, Limb-Girdle

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Source

Identifiers

PMID: 32925084
DOI: 10.3233/JND-200487

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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