Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CCDC28B[original query] |
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Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly. Journal of medical genetics 2017 11 55 (3): 189-197. Y?ld?z Bölükba?? Esra, Mumtaz Sara, Afzal Muhammad, Woehlbier Ute, Malik Sajid, Tolun Asl?h |
Clinical and Molecular Diagnosis of Joubert Syndrome and Related Disorders. Pediatric neurology 2020 3 106 43-49. Radha Rama Devi Akella, Naushad Shaik Mohammad, Lingappa Loke |
A CVID-associated variant in the ciliogenesis protein CCDC28B disrupts immune synapse assembly. Cell death and differentiation 2021 Jul . Capitani Nagaja, Onnis Anna, Finetti Francesca, Cassioli Chiara, Plebani Alessandro, Brunetti Jlenia, Troilo Arianna, D'Elios Sofia, Baronio Manuela, Gazzurelli Luisa, Della Bella Chiara, Billadeau Daniel D, D'Elios Mario Milco, Lougaris Vassilios, Baldari Cosima |
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- Page last updated:Apr 22, 2024
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