Perampanel markedly improved clinical seizures in a patient with a Rett‐like phenotype and 960‐kb deletion on chromosome 9q34.11 including the <i>STXBP1</i>-Reference-Cited by-同舟云学术

Perampanel markedly improved clinical seizures in a patient with a Rett‐like phenotype and 960‐kb deletion on chromosome 9q34.11 including the STXBP1

Published:2022-05 Issue:5 Volume:10 Page:
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clinical Case Reports

Author:

Yoshida Syun¹,Amamoto Masano¹,Takahashi Tomoyuki²,Tomita Ichiro¹,Yuge Kotaro³,Hara Munetsugu³,Iwama Kazuhiro⁴,Matsumoto Naomichi⁴,Matsuishi Toyojiro²⁵^ORCID

Affiliation:

1. Children’s Medical Center Kitakyushu City Yahata Hospital Kitakyushu Japan

2. Division of Gene Therapy and Regenerative Medicine Cognitive and Molecular Research Institute of Brain Diseases Kurume University School of Medicine Kurume Japan

3. Department of Pediatrics and Child Health Kurume University School of Medicine Fukuoka Japan

4. Department of Human Genetics Graduate School of Medicine Yokohama City University Kanagawa Japan

5. Research Center for Children and Research Center for Rett Syndrome St. Mary’s Hospital Fukuoka Japan

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.5811