Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients.

Alehabib, Elham; Esmaeilizadeh, Zahra; Ranji-Burachaloo, Sakineh; Tafakhori, Abbas; Darvish, Hossein; Movafagh, Abolfazl

Alehabib, Elham; Esmaeilizadeh, Zahra; Ranji-Burachaloo, Sakineh; Tafakhori, Abbas; Darvish, Hossein; Movafagh, Abolfazl.

Afiliação

Alehabib E; Student Research Committee, Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Esmaeilizadeh Z; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Ranji-Burachaloo S; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Tafakhori A; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Darvish H; Neuroscience Research Center, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Movafagh A; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. movafagh_a@yahoo.com.

Orphanet J Rare Dis ; 16(1): 461, 2021 11 02.

Article em En | MEDLINE | ID: mdl-34727962

Assuntos

Canais de Cálcio Tipo Q; Canais de Cálcio/genética; Epilepsia; Adolescente; Canais de Cálcio Tipo N/genética; Epilepsia/genética; Humanos; Estudos Retrospectivos

Palavras-chave

Brain imaging abnormalities; CACNA1A; Calcium channels; Epilepsy; Intellectual disability; Neurodevelopmental disorder

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canais de Cálcio / Canais de Cálcio Tipo Q / Epilepsia Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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