A female patient with childhood onset parkinsonism due to a truncating variant in the c terminal of the MECP2 gene

Harumi Saijo

Presentation information

General Oral Presentation

[O29] 遺伝・先天異常 1

Sat. Jun 1, 2024 8:30 AM - 9:30 AM Room8 (Bldg.1 3F 131＋132)

Organizer:Mie Inaba(Department of Pediatrics,Medical Genetics, Aichi Developmental Disability Center Central Hospital),Naoko Ishihara(Department of Pediatrics, Fujita Health University School of Medicine)

[O29-2] A female patient with childhood onset parkinsonism due to a truncating variant in the c terminal of the MECP2 gene

^○Harumi Saijo¹, Takanori Ezoe¹, Katsuhito Araki¹, Shinichi Kameyama², Hiromi Fukuda², Takeshi Mizuguchi², Naomichi Matsumoto² (1.Tokyo Metropolitan Higashiyamato Medical Center for Developmental/Multiple Disabilities, Tokyo, Japan, 2.Department of Human Genetics, Graduate School of Medicine, Yokohama City University, Kanagawa, Japan)

Abstract password authentication.
Password is required to view the abstract. Please enter a password to authenticate.