Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis-Reference-Cited by-同舟云学术

Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis

Published:2018-05-03 Issue:7 Volume:45 Page:862-866
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Leng Yunji¹,Yan Lulu¹,Feng Hongquan²,Chen Chen¹,Wang Shusen¹,Luo Yang¹,Cao Lihua¹^ORCID

Affiliation:

1. The Research Center for Medical Genomics, Key Laboratory of Cell Biology, Ministry of Public Health, Key Laboratory of Medical Cell Biology, Ministry of Education, College of Basic Medical Science; China Medical University; Shenyang China

2. The Research Center for Technology; Changqing Primary People's Court; Jinan China

Funder

National Natural Science Foundation of China

Department of Education of Liaoning Province

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.14343/fullpdf

Reference9 articles.

1. Porokeratosis ptychotropica: a clinically distinct variant of porokeratosis;McGuigan;J Am Acad Dermatol,2009

2. Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis;Zhang;Nat Genet,2012

3. Genomic variations of the mevalonate pathway in porokeratosis;Zhang;Elife,2015

4. Exome sequencing identifies SLC17A9 pathogenic gene in two Chinese pedigrees with disseminated superficial actinic porokeratosis;Cui;J Med Genet,2014

5. Mutations in the mevalonate pathway genes in Chinese patients with porokeratosis;Li;J Eur Acad Dermatol Venereol,2016

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