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Novel BRAT1 variant associated with neurodevelopmental disorder with cerebellar atrophy and seizure: Case report and a literature review.
Ghasemi, Mohammad-Reza; Tehrani Fateh, Sahand; Hashemi-Gorji, Farzad; Sheikhi Nooshabadi, Morteza; Alijanpour, Sahar; Mardi, Ali; Miryounesi, Mohammad.
Affiliation
  • Ghasemi MR; Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Tehrani Fateh S; Center for Comprehensive Genetic Services, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Hashemi-Gorji F; School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Sheikhi Nooshabadi M; Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Alijanpour S; School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Mardi A; Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Miryounesi M; Center for Comprehensive Genetic Services, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Epilepsy Behav Rep ; 27: 100702, 2024.
Article in En | MEDLINE | ID: mdl-39188779
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Epilepsy Behav Rep Year: 2024 Document type: Article Affiliation country: Irán Country of publication: Estados Unidos
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Epilepsy Behav Rep Year: 2024 Document type: Article Affiliation country: Irán Country of publication: Estados Unidos