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Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.
Yemni, Eman Al; Monies, Dorota; Alkhairallah, Thamer; Bohlega, Saeed; Abouelhoda, Mohamed; Magrashi, Amna; Mustafa, Abeer; AlAbdulaziz, Basma; Alhamed, Mohamed; Baz, Batoul; Goljan, Ewa; Albar, Renad; Jabaan, Amjad; Faquih, Tariq; Subhani, Shazia; Ali, Wafa; Shinwari, Jameela; Al-Mubarak, Bashayer; Al-Tassan, Nada.
Afiliação
  • Yemni EA; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Monies D; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, P.O Box 6086, Riyadh, 11442, Saudi Arabia.
  • Alkhairallah T; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, P.O Box 6086, Riyadh, 11442, Saudi Arabia.
  • Bohlega S; Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Abouelhoda M; Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Magrashi A; Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Mustafa A; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, P.O Box 6086, Riyadh, 11442, Saudi Arabia.
  • AlAbdulaziz B; Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Alhamed M; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Baz B; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Goljan E; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Albar R; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, P.O Box 6086, Riyadh, 11442, Saudi Arabia.
  • Jabaan A; Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Faquih T; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Subhani S; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, P.O Box 6086, Riyadh, 11442, Saudi Arabia.
  • Ali W; Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Shinwari J; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, P.O Box 6086, Riyadh, 11442, Saudi Arabia.
  • Al-Mubarak B; Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Al-Tassan N; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, P.O Box 6086, Riyadh, 11442, Saudi Arabia.
Sci Rep ; 9(1): 3344, 2019 03 04.
Article em En | MEDLINE | ID: mdl-30833663

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Variações do Número de Cópias de DNA / Sequenciamento do Exoma Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Sci Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Arábia Saudita

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Variações do Número de Cópias de DNA / Sequenciamento do Exoma Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Sci Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Arábia Saudita