P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2023-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774423001310 |
| _version_ | 1797342011318075392 |
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| author | Mohammed Almannai Lama AlAbdi Sateesh Maddirevula Maha Alotaibi Bader AlSaleem Yaser Aljadhai Hessa Alsaif Mussad Abu Khalid Fowzan Alkuraya |
| author_facet | Mohammed Almannai Lama AlAbdi Sateesh Maddirevula Maha Alotaibi Bader AlSaleem Yaser Aljadhai Hessa Alsaif Mussad Abu Khalid Fowzan Alkuraya |
| author_sort | Mohammed Almannai |
| collection | DOAJ |
| first_indexed | 2024-03-08T10:27:15Z |
| format | Article |
| id | doaj.art-1705b1ce361e426d969aa71b980d3d0f |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2024-03-08T10:27:15Z |
| publishDate | 2023-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-1705b1ce361e426d969aa71b980d3d0f2024-01-27T07:04:22ZengElsevierGenetics in Medicine Open2949-77442023-01-0111100131P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolonMohammed Almannai0Lama AlAbdi1Sateesh Maddirevula2Maha Alotaibi3Bader AlSaleem4Yaser Aljadhai5Hessa Alsaif6Mussad Abu Khalid7Fowzan Alkuraya8Genetics and Precision Medicine Department, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi ArabiaDepartment of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaDepartment of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaChildren’s Hospital, King Saud Medical City, Saudi ArabiaDivision of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi ArabiaDepartment of Neuroimaging and Intervention, Medical Imaging Administration, King Fahad Medical City, Riyadh, Saudi ArabiaCentre of Excellence for Biomedicine, Joint Centres of Excellence Program, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi ArabiaDepartment of Neuroscience, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaDepartment of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabiahttp://www.sciencedirect.com/science/article/pii/S2949774423001310 |
| spellingShingle | Mohammed Almannai Lama AlAbdi Sateesh Maddirevula Maha Alotaibi Bader AlSaleem Yaser Aljadhai Hessa Alsaif Mussad Abu Khalid Fowzan Alkuraya P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon Genetics in Medicine Open |
| title | P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon |
| title_full | P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon |
| title_fullStr | P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon |
| title_full_unstemmed | P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon |
| title_short | P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon |
| title_sort | p102 kif26a is mutated in the syndrome of congenital hydrocephalus with megacolon |
| url | http://www.sciencedirect.com/science/article/pii/S2949774423001310 |
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