The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology

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APPES/JSPE Joint Session(English)

APPES/JSPE Joint Session(English) » Tea Break&Poster Discussion

P1-8: Bone & minerals

Fri. Nov 18, 2016 10:15 AM - 10:45 AM Poster & Exhibition Room (Hall B5)

[P1-8-2] 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)

The password will be announced in the abstract book.

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