Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update.
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| Title: | Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update. |
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| Authors: | Maddirevula S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Shamseldin HE; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Sirr A; Pacific Northwest Research Institute, Seattle, WA, United States., AlAbdi L; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia., Lo RS; Pacific Northwest Research Institute, Seattle, WA, United States., Ewida N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Al-Qahtani M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Hashem M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Abdulwahab F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Aboyousef O; Department of Genetics, 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., Monies D; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Salem MH; Pediatric Nephrology Service, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia., Al Harbi N; Pediatric Nephrology Service, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia., Aldhalaan HM; Department of Neuroscience, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Alzaidan H; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Almanea HM; Anatomic Pathology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Alsalamah AK; Vitreoretinal and Uveitis Divisions, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia., Al Mutairi F; Medical Genetics Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Abdulaziz Medical City, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia., Ismail S; Human Genetics & Genome Research Division, Clinical Genetics Department, Center of Excellence of Human Genetics, National Research Centre, Cairo, Egypt., Abdel-Salam GMH; Human Genetics & Genome Research Division, Clinical Genetics Department, Center of Excellence of Human Genetics, National Research Centre, Cairo, Egypt., Alhashem A; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Department of Pediatric, Prince Sultan Medical Military City, Riyadh, Saudi Arabia., Asery A; Section of Pediatric Gastroenterology, Children's Specialist Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Faqeih E; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., AlQassmi A; Pediatric Neurology, King Saud Medical City, Riyadh, Saudi Arabia., Al-Hamoudi W; Department of Medicine, College of Medicine, King Saud University, Riyadh, Saudi Arabia., Algoufi T; King Faisal Specialist Hospital and Research Center, Organ Transplant Centre, Riyadh, Saudi Arabia., Shagrani M; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; King Faisal Specialist Hospital and Research Center, Organ Transplant Centre, Riyadh, Saudi Arabia., Dudley AM; Pacific Northwest Research Institute, Seattle, WA, United States., Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia. |
| Source: | Frontiers in genetics [Front Genet] 2020 Dec 31; Vol. 11, pp. 580484. Date of Electronic Publication: 2020 Dec 31 (Print Publication: 2020). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1664-8021 |
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| DOI: | 10.3389/fgene.2020.580484 |
