P1-8: Bone & minerals

[P1-8-2] [Poster Tour]A novel genetic syndrome caused by dominantly-inherited ORAI1 mutations: a combination of hypoparathyroidism and tubular aggregate myopathy

^○Rie Kawakita, Azumi Sakakibara, Yukiko Hashimoto, Yuki Hosokawa, Tohru Yorifuji (Division of Pediatric Endocrinology and Metabolism, Osaka City General Hospital)