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Article

The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication

1 Jun 1992

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1303230
DOI: 10.1038/ng0692-171

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The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplicationPMID 1303230Read ↗

The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1ASemantic proximity Read ↗

Charcot-Marie-Tooth disease type 1A: mutational mechanisms and candidate gene.Semantic proximity Read ↗

Charcot-Marie-Tooth caused by a copy number variation in myelin protein zero.Semantic proximity Read ↗

Exonic SNPs at positions 220 (A/G) and 445 (C/T) of the peripheral myelin protein 2 (PMP2).Semantic proximity Read ↗

Peripheral myelin protein 22: facts and hypotheses.Semantic proximity Read ↗

Many facets of the peripheral myelin protein PMP22 in myelination and disease.Semantic proximity Read ↗

Charcot-Marie-Tooth polyneuropathy: duplication, gene dosage, and genetic heterogeneity.Semantic proximity Read ↗

The PMP22 gene and its related diseases.Semantic proximity Read ↗

Copy number variation upstream of PMP22 in Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1.Semantic proximity Read ↗

Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.Semantic proximity Read ↗

Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations.Semantic proximity Read ↗

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