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Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.
Aldosary, Mazhor; Al-Bakheet, AlBandary; Al-Dhalaan, Hesham; Almass, Rawan; Alsagob, Maysoon; Al-Younes, Banan; AlQuait, Laila; Mustafa, Osama Mufid; Bulbul, Mustafa; Rahbeeni, Zuhair; Alfadhel, Majid; Chedrawi, Aziza; Al-Hassnan, Zuhair; AlDosari, Mohammed; Al-Zaidan, Hamad; Al-Muhaizea, Mohammad A; AlSayed, Moeenaldeen D; Salih, Mustafa A; AlShammari, Mai; Faiyaz-Ul-Haque, Muhammad; Chishti, Mohammad Azhar; Al-Harazi, Olfat; Al-Odaib, Ali; Kaya, Namik; Colak, Dilek.
Afiliação
  • Aldosary M; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Al-Bakheet A; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Al-Dhalaan H; Department of Neuroscience, and King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Almass R; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Alsagob M; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Al-Younes B; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • AlQuait L; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Mustafa OM; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Bulbul M; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Rahbeeni Z; Department of Medical Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Alfadhel M; King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, Genetics Division, Department of Pediatrics, King Abdullah Specialized Children Hospital, Riyadh, Saudi Arabia.
  • Chedrawi A; Department of Neuroscience, and King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Al-Hassnan Z; Department of Medical Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • AlDosari M; Center for Pediatric Neurosciences, Cleveland Clinic, Cleveland, Ohio.
  • Al-Zaidan H; Department of Medical Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Al-Muhaizea MA; Department of Neuroscience, and King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • AlSayed MD; Department of Medical Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Salih MA; Division of Pediatric Neurology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • AlShammari M; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Faiyaz-Ul-Haque M; Department of Pathology and King Khalid Hospital, King Saud University, Riyadh, Saudi Arabia.
  • Chishti MA; Department of Biochemistry, King Khalid Hospital, King Saud University, Riyadh, Saudi Arabia.
  • Al-Harazi O; Department of Biostatistics, Epidemiology, and Scientific Computing, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Odaib A; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Kaya N; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Colak D; Department of Biostatistics, Epidemiology, and Scientific Computing, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
OMICS ; 24(3): 160-171, 2020 03.
Article em En | MEDLINE | ID: mdl-32105570
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Rett / Proteínas Serina-Treonina Quinases / Proteína 2 de Ligação a Metil-CpG / Fatores de Transcrição Forkhead / Genoma Mitocondrial / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Rett / Proteínas Serina-Treonina Quinases / Proteína 2 de Ligação a Metil-CpG / Fatores de Transcrição Forkhead / Genoma Mitocondrial / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2020 Tipo de documento: Article