A newKRT16mutation associated with a phenotype of pachyonychia congenita-Reference-Cited by-同舟云学术

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A newKRT16mutation associated with a phenotype of pachyonychia congenita

Published:2013-11-27 Issue:12 Volume:22 Page:838-839
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

Paris Francesc¹,Hurtado Cristina¹,Azón Antoni²,Aguado Leyre³,Vizmanos José L.¹

Affiliation:

1. Department of Biochemistry & Genetics; School of Sciences; University of Navarra; Pamplona Spain

2. Department of Dermatology; University Hospital Sant Joan; Universitat Rovira i Virgili; Reus Spain

3. Department of Dermatology; Clínica Universidad de Navarra; Pamplona Spain

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/exd.12262/fullpdf

Reference20 articles.

1. The Phenotypic and Molecular Genetic Features of Pachyonychia Congenita

2. The Genetic Basis of Pachyonychia Congenita

3. Keratin K6c Mutations Cause Focal Palmoplantar Keratoderma

4. Keratin 16 and keratin 17 mutations cause pachyonychia congenita

5. Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families

Cited by 4 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. Mutation p.Arg127Pro in the 1A Domain of KRT16 Causes Pachyonychia Congenita in Chinese Patient: A Case Report of PC Associated with Acral Melanoma;Clinical, Cosmetic and Investigational Dermatology;2024-05

2. Revisiting pachyonychia congenita: a case‐cohort study of 815 patients;British Journal of Dermatology;2020-01-14

3. A KRT16 mutation in the first Chinese pedigree with Pachyonychia congenita and review of the literatures;Journal of Cosmetic Dermatology;2019-03-12

4. Pachyonychia Congenita (K16) with Unusual Features and Good Response to Acitretin;Case Reports in Dermatology;2015-08-19

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