Literature DB >> 18547302

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.

T Tsuda1, C Ishikawa, N Nakagawa, H Konishi, M Tarutani, M Matsuki, K Yamanishi.   

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Year:  2008        PMID： 18547302     DOI： 10.1111/j.1365-2133.2008.08684.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  1 in total

1.  Keratin 17 Mutations in Four Families from India with Pachyonychia Congenita.

Authors:  Manoj Agarwala; Pankaj Salphale; Dincy Peter; Neil J Wilson; Susanne Pulimood; Mary E Schwartz; Frances J D Smith
Journal:  Indian J Dermatol       Date:  2017 Jul-Aug       Impact factor: 1.494
  1 in total

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