Publication Date:
2015-07-17
Description:
Article Alpha-1 antitrypsin deficiency is a common genetic disorder in Europeans. Here Setoh et al . perform a genome-wide association study of AAT serum levels in a Japanese population and find three missense variants in the metabolism genes ALDH2 , HNF1A and GCKR . Nature Communications doi: 10.1038/ncomms8754 Authors: Kazuya Setoh, Chikashi Terao, Shigeo Muro, Takahisa Kawaguchi, Yasuharu Tabara, Meiko Takahashi, Takeo Nakayama, Shinji Kosugi, Akihiro Sekine, Ryo Yamada, Michiaki Mishima, Fumihiko Matsuda
Electronic ISSN:
2041-1723
Topics:
Biology
,
Chemistry and Pharmacology
,
Natural Sciences in General
,
Physics
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