Prevalent LIPH founder mutations lead to loss of P2Y5...

Human Mutation 2010 Vol. 31; Iss. 5

Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1α in autosomal recessive hypotrichosis

Satoru Shinkuma, Masashi Akiyama, Asuka Inoue, Junken Aoki, Ken Natsuga, Toshifumi Nomura, Ken Arita, Riichiro Abe, Kei Ito, Hideki Nakamura, Hideyuki Ujiie, Akihiko Shibaki, Hiraku Suga, Yuichiro Tsu
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Volume:
31
Year:
2010
Language:
english
Pages:
1
DOI:
10.1002/humu.21235
File:
PDF, 522 KB
english, 2010
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