Your browser doesn't support javascript.
loading
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.
Bohlega, Saeed A; Al-Mubarak, Bashayer R; Alyemni, Eman A; Abouelhoda, Mohamed; Monies, Dorota; Mustafa, Abeer E; Khalil, Dania S; Al Haibi, Sara; Abou Al-Shaar, Hussam; Faquih, Tariq; El-Kalioby, Mohamed; Tahir, Asma I; Al Tassan, Nada A.
Afiliación
  • Bohlega SA; Department of Neurosciences, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Al-Mubarak BR; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia. BAl-Mubarak@kfshrc.edu.sa.
  • Alyemni EA; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Abouelhoda M; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Monies D; Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Mustafa AE; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Khalil DS; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Al Haibi S; Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Abou Al-Shaar H; Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Faquih T; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • El-Kalioby M; Department of Neurosciences, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
  • Tahir AI; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Al Tassan NA; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
BMC Res Notes ; 9: 295, 2016 Jun 07.
Article en En | MEDLINE | ID: mdl-27268037
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Heterogeneidad Genética / Mutación Missense / Trastornos Parkinsonianos / Fosfolipasas A2 Grupo VI Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: BMC Res Notes Año: 2016 Tipo del documento: Article País de afiliación: Arabia Saudita
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Heterogeneidad Genética / Mutación Missense / Trastornos Parkinsonianos / Fosfolipasas A2 Grupo VI Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: BMC Res Notes Año: 2016 Tipo del documento: Article País de afiliación: Arabia Saudita