Identification of a Germline Mutation in Keratin 17 in a Family with Pachyonychia Congenita Type 2-Reference-Cited by-同舟云学术

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Identification of a Germline Mutation in Keratin 17 in a Family with Pachyonychia Congenita Type 2

Published:1999-11 Issue:5 Volume:113 Page:848-850
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Çelebi Julide Tok,Yao Ya Juan,Peacocke Monica,Tanzi Elizabeth L.,Michael Elias J.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference15 articles.

1. Mutation of a type II keratin gene (K6a) in pachyonychia congenita;Bowden;Nat Genet,1995

2. Human keratin diseases: hereditary fragility of specific epithelial tissues;Corden;Exp Dermatol,1996

3. Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2;Covello;Br J Dermatol,1998

4. Intermediate filaments: structure, dynamics, function and disease;Fuchs;Annu Rev Biochem,1994

5. Pachyonychia congenita type 2: keratin 17 mutation in a Japanese case;Fujimoto;J Am Acad Dermatol,1998

Cited by 23 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. Pachyonychia Congenita;Atlas of Genetic Diagnosis and Counseling;2017

2. Pachyonychia Congenita;Atlas of Genetic Diagnosis and Counseling;2016

3. Steatocystoma multiplex: keratin 17 – the key player?;British Journal of Dermatology;2012-11-26

4. Pachyonychia Congenita;Atlas of Genetic Diagnosis and Counseling;2012

5. 9 Disorders of epidermal maturation and keratinization;Weedon's Skin Pathology;2010

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