Spinal muscular atrophy—like features in a child with heterozygous MYBPC1 mutations

Saki Uneoka

講演情報

Platform Session

[EO-02] Platform Session 02：Neuromuscular Disorders 2

2022年6月2日(木) 13:10 〜 14:20 第6会場 (2F 中会議室202)

Chair: Yi Fong Choong(Department of Paediatrics, Faculty of Medicine, Un),Takahiro Yonekawa(Department of Pediatrics, Mie University Graduate School of Medicine)

[EO-008] Spinal muscular atrophy—like features in a child with heterozygous MYBPC1 mutations

Saki Uneoka¹，Yurika Numata—Uematsu¹，Yu Abe¹，Naoya Saijo¹，Yu Aihara¹，Yu Katata¹，Yoshitsugu Oikawa¹，Mitsugu Uematsu¹，Kayoko Saito²，Shigeo Kure¹ (1. Department of Pediatrics, University of Tohoku, Miyagi, Japan，2. Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan)

抄録パスワード認証
パスワードは、「第64回日本小児神経学会学術集会プログラム・抄録集」（「脳と発達」第54巻学術集会号）に記載してあります。