☆ 4.6 Article

A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb

BRITISH JOURNAL OF DERMATOLOGY (2008)

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Journal

BRITISH JOURNAL OF DERMATOLOGY
Volume 159, Issue 3, Pages 730-732

Publisher

WILEY
DOI: 10.1111/j.1365-2133.2008.08684.x

Keywords

hair bulb; keratin 17; pachyonychia congenita; point mutation; RNA

Categories

Dermatology

Funding

  1. High-Tech Research Center

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