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Congenital disorders of glycosylation: The Saudi experience
Authors:Sarah Alsubhi  Amal Alhashem  Eissa Faqeih  Majid Alfadhel  Abdullah Alfaifi  Waleed Altuwaijri  Saud Alsahli  Hesham Aldhalaan  Fowzan S. Alkuraya  Khalid Hundallah  Adel Mahmoud  Ali Alasmari  Fuad Al Mutairi  Hanem Abduraouf  Layan AlRasheed  Saad Alshahwan  Brahim Tabarki
Affiliation:1. Division of Pediatric Neurology, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia;2. Division of Genetics, Department of Pediatrics;3. Prince Sultan Military Medical City, Riyadh, Saudi Arabia;4. Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia;5. Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia;6. Division of Pediatric Neurology, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia;7. Division of Pediatric Neurology, Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia;8. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia;9. Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
Abstract:
Keywords:ALG9  CDG  Congenital disorder(s) of glycosylation  severe phenotype  skeletal dysplasia
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