○Moriei Shibuya1,2, Haruhiko Nakamura1,5, Naoya Saijyo1, Saki Uneoka1, Yuusuke Takezawa1, Yoshitugu Oikawa1, Yurika Uematsu1, Mitsugu Uematsu1, Jyun Takayama3,4, Shigeo Kure3,5, Gen Tamiya3,4, Atsuo Kikuchi1,3
(1.Department of Pediatrics, University of Tohoku, Sendai, Japan, 2.Yamagata prefectural central hospital, Yamagata, Japan., 3.Department of Genome Analysis for Rare and Intractable Diseases,University of Tohoku,Sendai,Japan, 4.RIKEN Center for Advanced Intelligence Project Statistical Genetics Team,Tokyo,Japan, 5.Miyagi prefectural children hospital)
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