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ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder.
Al-Hassnan, Zuhair N; Al-Dosary, Mazhor; Alfadhel, Majid; Faqeih, Eissa A; Alsagob, Maysoon; Kenana, Rosan; Almass, Rawan; Al-Harazi, Olfat S; Al-Hindi, Hindi; Malibari, Omhani I; Almutari, Faten B; Tulbah, Sahar; Alhadeq, Faten; Al-Sheddi, Tarfa; Alamro, Rana; AlAsmari, Ali; Almuntashri, Makki; Alshaalan, Hesham; Al-Mohanna, Futwan A; Colak, Dilek; Kaya, Namik.
Affiliation
  • Al-Hassnan ZN; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Al-Dosary M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alfadhel M; Genetics Division, Department of Pediatrics, King Saud bin Abdulaziz University for Health Science, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Faqeih EA; Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Alsagob M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Kenana R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Almass R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Harazi OS; Department of Biostatistics and Scientific Computing, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Hindi H; Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Malibari OI; Pediatrics Department, King Abdullah Medical City, Maternity & Children's Hospital, Al-Madinah al-Munawarah, Riyadh, Saudi Arabia.
  • Almutari FB; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Tulbah S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alhadeq F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Sheddi T; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alamro R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • AlAsmari A; Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Almuntashri M; Department of Radiology, King Abdulaziz Medical City, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Alshaalan H; Department of Radiology, King Abdulaziz Medical City, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Al-Mohanna FA; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia Department of Cell Biology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Colak D; Department of Biostatistics and Scientific Computing, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Kaya N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia Department of Biostatistics and Scientific Computing, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
J Med Genet ; 52(3): 186-94, 2015 Mar.
Article in En | MEDLINE | ID: mdl-25539947
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neurodegenerative Diseases / Mitochondrial Diseases / Alexander Disease / Iron-Sulfur Proteins Type of study: Etiology_studies Limits: Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: J Med Genet Year: 2015 Type: Article Affiliation country: Saudi Arabia
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neurodegenerative Diseases / Mitochondrial Diseases / Alexander Disease / Iron-Sulfur Proteins Type of study: Etiology_studies Limits: Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: J Med Genet Year: 2015 Type: Article Affiliation country: Saudi Arabia