Published in
Oxford University Press (OUP), Human Molecular Genetics, 3(24), p. 637-648, 2014
DOI: 10.1093/hmg/ddu477
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Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca2+ channels
Journal article published in 2014 by
Yukari Endo,
Satoru Noguchi,
Yuji Hara,
Yukiko K. Hayashi,
Kazushi Motomura,
Satoko Miyatake,
Nobuyuki Murakami,
Satsuki Tanaka,
Sumimasa Yamashita,
Rika Kizu,
Masahiro Bamba,
Yu-Ichi Goto,
Naomichi Matsumoto,
Ikuya Nonaka,
Ichizo Nishino 
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