Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria-Reference-Cited by-同舟云学术

Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria

Published:2021-05-24 Issue: Volume: Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Liu Jia‐Wei¹^ORCID,Habulieti Xiaerbati²,Wang Rong‐rong²,Ma Dong‐Lai¹,Zhang Xue²

Affiliation:

1. Department of Dermatology Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, National Clinical Research Center for Skin and Immune Diseases Beijing China

2. Mckusick‐Zhang Center for Genetic Medicine State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23803

Reference22 articles.

1. Mutations in ABCB6 cause dyschromatosis universalis hereditaria;Zhang C;J Invest Dermatol,2013

2. Dyschromatosis universalis hereditaria;Sethuraman G;Clin Exp Dermatol,2002

3. Dyschromatosis universalis hereditaria: a case report;Udayashankar C;Dermatol Online J,2011

4. Dyschromatosis universalis hereditaria: report of a case and review of the literature;Al Hawsawi K;Pediatr Dermatol,2002

5. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family;Bukhari IA;J Eur Acad Dermatol Venereol,2006

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