Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: C8orf37[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 |
Identification of nine novel loci related to hematological traits in a Japanese population. Physiological genomics 2018 Sep 50 (9): 758-769. Yasukochi Yoshiki, Sakuma Jun, Takeuchi Ichiro, Kato Kimihiko, Oguri Mitsutoshi, Fujimaki Tetsuo, Horibe Hideki, Yamada Yoshi |
A nonsense mutation in C8orf37 linked with retinitis pigmentosa, early macular degeneration, cataract, and myopia in an arRP family from North India. BMC ophthalmology 2023 5 23 (1): 210. Shiwali Goyal, Kabir Singh, Aashna Uppal, Vanita Vani |
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- Page last updated:Apr 22, 2024
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