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Article

Mutation E402K of the hHb6 in a Chinese Han family with monilethrix.

European journal of dermatology : EJD - 1 Jan 2000

ZHANG Shi-de, MENG Jin, ZHAO Jing-Jun, TIAN Wei

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19505862
DOI: 10.1684/ejd.2009.0717

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Related research

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Mutation E402K of the hHb6 in a Chinese Han family with monilethrix.PMID 19505862Read ↗

[Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].Semantic proximity Read ↗

Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family.Semantic proximity Read ↗

Two different mutations in the same codon of a type II hair keratin (hHb6) in patients with monilethrix.Semantic proximity Read ↗

A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin.Semantic proximity Read ↗

A missense mutation in the type II hair keratin hHb3 is associated with monilethrix.Semantic proximity Read ↗

A novel mutation in K6b in pachyonychia congenita type 2.Semantic proximity Read ↗

Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene.Semantic proximity Read ↗

A recurrent mutation of GJB6 in a big Chinese family with Hidrotic ectodermal dysplasia.Semantic proximity Read ↗

A CMT2 family carrying the P7R mutation in the N- terminal region of the HSPB1 gene.Semantic proximity Read ↗

Rare MPIG6B Gene Mutation in an Indian Male with Anemia and ThrombocytopeniaSemantic proximity Read ↗

A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1.Semantic proximity Read ↗

De novo mutations in monilethrix.Semantic proximity Read ↗

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