A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosis

Clin Exp Dermatol. 2013 Oct;38(7):796-8. doi: 10.1111/ced.12129. Epub 2013 Jun 18.

Authors

L H Liu¹, G Chen, J W Wang, S X Liu, J B Wang, F S Zhou, J Zhu, L D Sun, M Gao, P G Wang, S Yang, X J Zhang

Affiliation

¹ Institute of Dermatology, Anhui Medical University, Hefei, 230032, Anhui, China; State Key Laboratory Incubation Base of Dermatology, Ministry of National Science and Technology, Hefei, Anhui, China; Key Laboratory of Dermatology, Ministry of Education, Hefei, Anhui, China.

PMID: 23773027
DOI: 10.1111/ced.12129

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Consanguinity*
Hair / abnormalities*
Hair Diseases / genetics*
Humans
Hypotrichosis / genetics*
Male
Receptors, Lysophosphatidic Acid / genetics*
Sequence Deletion*

Substances

LPAR6 protein, human
Receptors, Lysophosphatidic Acid

Supplementary concepts

Woolly Hair, Autosomal Recessive