Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Hadeel Salah Kashan"'
Autor:
Hadeel Salah Kashan, Afraa Mohamed Albakrye, Hind Abdelaziz Elnasri, Mona Abdelrahman Mohamed Khaier
Publikováno v:
Informatics in Medicine Unlocked, Vol 27, Iss , Pp 100808- (2021)
Introduction: Dopa responsive dystonia (DRD) is an inherited movement disorder. Mutations in GCH1 gene is the most common root of autosomal dominant, early onset of DRD. This study aimed to analyze the genetic variation that can alter the expression
Externí odkaz:
https://doaj.org/article/94e6c36e5f8c479b807ad11be239b8bb
Autor:
Mona Abdelrahman Mohamed Khaier, Hind Abdelaziz Elnasri, Hadeel Salah Kashan, Afra Mohamed Albkrye
Publikováno v:
Informatics in Medicine Unlocked, Vol 27, Iss, Pp 100808-(2021)
Introduction Dopa responsive dystonia (DRD) is an inherited movement disorder. Mutations in GCH1 gene is the most common root of autosomal dominant, early onset of DRD. This study aimed to analyze the genetic variation that can alter the expression a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89b33f12ac45d2beeb2202b2fa42b515
https://doi.org/10.1016/j.imu.2021.100808
https://doi.org/10.1016/j.imu.2021.100808