Molecular epidemiology of pachyonychia congenita in the Israeli population-Reference-Cited by-同舟云学术

Molecular epidemiology of pachyonychia congenita in the Israeli population

Published:2020-12-20 Issue:4 Volume:46 Page:663-668
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Pavlovsky M.¹^ORCID,Peled A.¹^ORCID,Samuelov L.¹²,Malki L.²,Malovitski K.²,Assaf S.²,Mohamad J.¹²,Meijers O.¹,Eskin‐Schwartz M.³,Sarig O.¹^ORCID,Sprecher E.¹²

Affiliation:

1. Division of Dermatology Tel Aviv Sourasky Medical Center Tel Aviv Israel

2. Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel

3. Genetics Institute at Soroka University Medical Center and Faculty of Health Sciences Ben‐Gurion University of the Negev Beer‐Sheva Israel

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ced.14509

Reference25 articles.

1. Mutation of a type II keratin gene (K6a) in pachyonychia congenita

2. Keratin 16 and keratin 17 mutations cause pachyonychia congenita

3. A Mutation in Human Keratin K6b Produces a Phenocopy of the K17 Disorder Pachyonychia Congenita Type 2

4. Keratin K6c Mutations Cause Focal Palmoplantar Keratoderma

5. Clinical and Pathological Features of Pachyonychia Congenita

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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. KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies;European Journal of Human Genetics;2022-06-09