Analysis of unique mutations in the LPAR6 gene identified in a Japanese family with autosomal recessive woolly hair/hypotrichosis: Establishment of a useful assay system for LPA6-Reference-Cited by-同舟云学术

Analysis of unique mutations in the LPAR6 gene identified in a Japanese family with autosomal recessive woolly hair/hypotrichosis: Establishment of a useful assay system for LPA6

Published:2015-06 Issue:3 Volume:78 Page:197-205
ISSN:0923-1811
Container-title:Journal of Dermatological Science
language:en
Short-container-title:Journal of Dermatological Science

Author:

Hayashi Ryota,Inoue Asuka,Suga Yasushi,Aoki Junken,Shimomura Yutaka

Funder

Takeda Science Foundation, Japan

Research on Measures for Intractable Diseases

Ministry of Health, Labour, and Welfare, Japan

PRESTO

Japan Science and Technology Agency

Grant-in-Aid for Scientific Research

JST

Grant-in-Aid for Scientific Research on Innovative Areas

MEXT

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference39 articles.

1. Congenital hair loss disorders: rare, but not too rare;Shimomura;J Dermatol,2012

2. Biology and genetics of hair;Shimomura;Annu Rev Genomics Hum Genet,2010

3. Founder mutations in the lipase H (LIPH) gene in families with autosomal recessive woolly hair/hypotrichosis;Shimomura;J Invest Dermatol,2009

4. Autosomal dominant woolly hair resulting from disruption of keratin 74 (KRT74), a novel determinant of human hair texture;Shimomura;Am J Hum Genet,2010

5. A missense mutation within the helix initiation motif of the keratin K71 gene underlies autosomal dominant woolly hair/hypotrichosis;Fujimoto;J Invest Dermatol,2012

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