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A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis.
Daneshmandpour, Yousef; Bahmanpour, Zahra; Kazeminasab, Somayeh; Aghaei Moghadam, Ehsan; Alehabib, Elham; Chapi, Marjan; Tafakhori, Abbas; Aghaei, Negar; Darvish, Hossein; Emamalizadeh, Babak.
Afiliação
  • Daneshmandpour Y; Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Bahmanpour Z; Cytogene Genetic Diagnostic Laboratory, Tabriz, Iran.
  • Kazeminasab S; Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Aghaei Moghadam E; Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Alehabib E; Department of Pediatrics, School of Medicine, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Chapi M; Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Tafakhori A; Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Aghaei N; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Darvish H; Research Center of Psychiatry and Behavioral Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Emamalizadeh B; Neuroscience Research Center, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Article em En | MEDLINE | ID: mdl-35852402

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article