TOPICS

5月の掲載論文・受賞

・内分泌グループ
Two siblings with congenital central hypothyroidism caused by a novel mutation in the IGSF1 gene
Makiko Oguma, Mizuki Kobayashi, Masayo Yamazaki, Koji Yokoyama, Shuntaro Morikawa, Takeshi Yamaguchi, Takanori Yamagata, and Toshihiro Tajima
Clin Pediatr Endocrinol 2018; 27(2), 95–100