Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family-Reference-Cited by-同舟云学术

Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family

Published:2019-02-27 Issue:5 Volume:46 Page:413-417
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Huang Ye¹^ORCID,Cai Chuan²,Ren Li³,Cui Caijuan¹,Zhang Xue⁴,Liu Wei¹

Affiliation:

1. Department of Dermatology Air Force General Hospital Chinese People's Liberation Army Beijing China

2. Institute of Stomatology Chinese People's Liberation Army General Hospital Beijing China

3. Department of Pathology Air Force General Hospital Chinese People's Liberation Army Beijing China

4. McKusick‐Zhang Center for Genetic Medicine Institute of Basic Medical Sciences Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China

Funder

Research Foundation of Air Force General Hospital

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.14811

Reference10 articles.

1. Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis

2. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

3. Identification of a Novel Locus for Marie Unna Hereditary Hypotrichosis to a 17.5 cM Interval at 1p21.1–1q21.3

4. A novel mutation of CYLD in a Chinese family with multiple familial trichoepithelioma

5. A New Cylindromatosis (CYLD) Gene Mutation in a Case of Brooke-Spiegler Syndrome Masquerading as Basal Cell Carcinoma of the Eyelids

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1. <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case;Current Pediatrics;2023-11-05

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