Novel

BRAT1 gene Neurodevelopmental disorders Neurological abnormalities Sanger sequencing Whole exome sequencing (WES)

Journal

Epilepsy & behavior reports
ISSN: 2589-9864
Titre abrégé: Epilepsy Behav Rep
Pays: United States
ID NLM: 101750909

Informations de publication

Date de publication:
2024
Historique:
received: 30 12 2023
revised: 29 07 2024
accepted: 29 07 2024
medline: 27 8 2024
pubmed: 27 8 2024
entrez: 27 8 2024
Statut: epublish

Résumé

The

Identifiants

pubmed: 39188779
doi: 10.1016/j.ebr.2024.100702
pii: S2589-9864(24)00059-5
pmc: PMC11345683
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100702

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Mohammad-Reza Ghasemi (MR)

Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Center for Comprehensive Genetic Services, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Sahand Tehrani Fateh (S)

School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Farzad Hashemi-Gorji (F)

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Morteza Sheikhi Nooshabadi (M)

School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Sahar Alijanpour (S)

Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Ali Mardi (A)

Center for Comprehensive Genetic Services, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Mohammad Miryounesi (M)

Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Classifications MeSH