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

Presentation information

APPES/JSPE Joint Session(English)

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

P1-4: Growth

Fri. Nov 18, 2016 2:45 PM - 3:35 PM Poster & Exhibition Room (Hall B5)

[P1-4-13] A Novel de novo Germline Mutation Glu40Lys in AKT3 causes Megalencephaly with Growth Hormone Deficiency.

Nagahara Keiko1,2, Masaki Takagi1,3, Takanari Fujii2, Gen Nishimura4, Mitsuhiro Kato2, Kazushige Dobashi2, Kazuo Itabashi2, Satoshi Narumi3, Tomonobu Hasegawa3 (1.Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, 2.Department of Pediatrics, Showa University School of Medicine, 3.Department of Pediatrics, Keio University School of Medicine, 4.Department of Radiology, Tokyo Metropolitan Children's Medical Center)

The password will be announced in the abstract book.

Password