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

Abstract Background Woolly hair (WH) is a hair shaft anomaly characterized by tightly-curled hair and is frequently associated with hypotrichosis. Non-syndromic forms of WH can show either autosomal dominant or recessive inheritance. The autosomal recessive form of WH (ARWH) is caused by mutations i...

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Veröffentlicht in:	Journal of dermatological science 2015-06, Vol.78 (3), p.197-205
Hauptverfasser:	Hayashi, Ryota, Inoue, Asuka, Suga, Yasushi, Aoki, Junken, Shimomura, Yutaka
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Dermatology Hair - abnormalities Hair Diseases - genetics HEK293 Cells Humans Hypotrichosis LIPH LPA6 LPAR6 Male Mutation Promoter Regions, Genetic Receptors, Lysophosphatidic Acid - genetics Woolly hair
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