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Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family.
Elsayed, Liena E O; Mohammed, Inaam N; Hamed, Ahlam A A; Elseed, Maha A; Salih, Mustafa A M; Yahia, Ashraf; Abubaker, Rayan; Koko, Mahmoud; Abd Allah, Amal S I; Elbashir, Mustafa I; Ibrahim, Muntaser E; Brice, Alexis; Ahmed, Ammar E; Stevanin, Giovanni.
Afiliação
  • Elsayed LEO; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
  • Mohammed IN; College of Medicine, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
  • Hamed AAA; Institut du Cerveau, INSERM, CNRS, Sorbonne Université, Paris, France.
  • Elseed MA; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
  • Salih MAM; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
  • Yahia A; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
  • Abubaker R; Division of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Koko M; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
  • Abd Allah ASI; Institut du Cerveau, INSERM, CNRS, Sorbonne Université, Paris, France.
  • Elbashir MI; Department of Biochemistry, Faculty of Medicine, National University, Khartoum, Sudan.
  • Ibrahim ME; Ecole Pratique des Hautes Etudes, EPHE, PSL Research University, Paris, France.
  • Brice A; Department of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan.
  • Ahmed AE; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, Tuebingen, Germany.
  • Stevanin G; Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
Front Neurol ; 11: 569996, 2020.
Article em En | MEDLINE | ID: mdl-33193012

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article