Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation-Reference-Cited by-同舟云学术

Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation

Published:2024-04 Issue:4 Volume:111 Page:761-777
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bhat Shreyas,Rousseau Justine,Michaud Coralie,Lourenço Charles Marques,Stoler Joan M.,Louie Raymond J.,Clarkson Lola K.,Lichty Angie,Koboldt Daniel C.,Reshmi Shalini C.,Sisodiya Sanjay M.,Hoytema van Konijnenburg Eva M.M.,Koop Klaas,van Hasselt Peter M.,Démurger Florence,Dubourg Christèle,Sullivan Bonnie R.,Hughes Susan S.,Thiffault Isabelle,Tremblay Elisabeth Simard,Accogli Andrea,Srour Myriam,Blunck Rikard,Campeau Philippe M.^ORCID

Funder

Canadian Institutes of Health Research

Natural Sciences and Engineering Research Council of Canada

Ontario Genomics Institute

Fonds de recherche du Quebec Sante

Epilepsy Society

Genome British Columbia

Digital Research Alliance of Canada

Génome Québec

Ontario Research Foundation

Genome Alberta

NIHR Great Ormond Street Hospital Biomedical Research Centre