PrevalentLIPHfounder mutations lead to loss of P2Y5 activation ability of PA-PLA1α in autosomal recessive hypotrichosis-Reference-Cited by-同舟云学术

PrevalentLIPHfounder mutations lead to loss of P2Y5 activation ability of PA-PLA1α in autosomal recessive hypotrichosis

Published:2010 Issue: Volume: Page:n/a-n/a
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Shinkuma Satoru,Akiyama Masashi,Inoue Asuka,Aoki Junken,Natsuga Ken,Nomura Toshifumi,Arita Ken,Abe Riichiro,Ito Kei,Nakamura Hideki,Ujiie Hideyuki,Shibaki Akihiko,Suga Hiraku,Tsunemi Yuichiro,Nishie Wataru,Shimizu Hiroshi

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21235/fullpdf

Reference30 articles.

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4. Structural basis for the substrate selectivity of pancreatic lipases and some related proteins;Carriere;Biochim Biophys Acta,1998

5. Detection of K-ras mutations in DNAs isolated from feces of patients with colorectal tumors by mutant-allele-specific amplification (MASA);Hasegawa;Oncogene,1995

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