Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2-Reference-Cited by-同舟云学术

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Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2

Published:2008-03-18 Issue:5 Volume:300 Page:211-214
ISSN:0340-3696
Container-title:Archives of Dermatological Research
language:en
Short-container-title:Arch Dermatol Res

Author:

Oh Adib Carol,Jones Brad,Liao Haihui,Smith Frances J. D.,Solomon Rustum,Egan Conleth A.,Leachman Sancy

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00403-008-0840-7.pdf

Reference28 articles.

1. Achten G, Wanet-Rouard J (1970) Pachyonychia. Br J Dermatol 83:56–62

2. Benjamin B, Parsons DS, Molloy HF (1987) Pachyonychia congenita with laryngeal involvement. Int J Pediatr Otorhinolaryngol 13:205–209

3. Bowden PE, Haley JL, Kansky A et al (1995) Mutation of a type II keratin gene (K6a) in pachyonychia congenita. Nat Genet 10:363–365

4. Celebi JT, Tanzi EL, Yao YJ et al (1999) Identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2. J Invest Dermatol 113:848–850

5. Clementi M, Cardin de Stefani E, Dei Rossi C et al (1986) Pachyonychia congenita Jackson-Lawler type: a distinct malformation syndrome. Br J Dermatol 114:367–370

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Keratin 17 in disease pathogenesis: from cancer to dermatoses;The Journal of Pathology;2018-12-07

2. A Large Mutational Study in Pachyonychia Congenita;Journal of Investigative Dermatology;2011-05

3. Keratin gene mutations in disorders of human skin and its appendages;Archives of Biochemistry and Biophysics;2011-04

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