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Article

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

1 Feb 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9462747
DOI: 10.1038/ng0298-164

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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyPMID 9462747Read ↗

GCG repeats and phenotype in oculopharyngeal muscular dystrophy.Semantic proximity Read ↗

Oculopharyngeal muscular dystrophy.Semantic proximity Read ↗

Oculopharyngeal muscular dystrophy (OPMD): analysis of the PABPN1 gene expansion sequence in 86 patients reveals 13 different expansion types and further evidence for unequal recombination as the mutational mechanism.Semantic proximity Read ↗

A GCG expansion (GCG)₁₁ in polyadenylate-binding protein nuclear 1 gene caused oculopharyngeal muscular dystrophy in a Chinese family.Semantic proximity Read ↗

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal MyopathySemantic proximity Read ↗

Mitochondrial localization of PABPN1 in oculopharyngeal muscular dystrophySemantic proximity Read ↗

Study of a Taiwanese family with oculopharyngeal muscular dystrophy.Semantic proximity Read ↗

[From gene to disease; the PABN1 gene and oculopharyngeal muscular dystrophy].Semantic proximity Read ↗

Oculopharyngeal muscular dystrophy (OPMD) due to a small duplication in the PABPN1 gene.Semantic proximity Read ↗

Late onset oculopharyngeal muscular dystrophy with prominent neurogenic features and short GCG trinucleotide expansion.Semantic proximity Read ↗

Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK population.Semantic proximity Read ↗

Identification of a novel mutation in a Korean patient with oculopharyngeal muscular dystrophy.Semantic proximity Read ↗

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