Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Vision and TRPM1[original query] |
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Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse. Equine veterinary journal 2020 7 53 (2): 316-323. Hack Yael L, Crabtree Elizabeth E, Avila Felipe, Sutton Roger B, Grahn Robert, Oh Annie, Gilger Brian, Bellone Rebecca |
Clinical and genetic findings in TRPM1-related congenital stationary night blindness. Acta ophthalmologica 2022 5 100 (6): e1332-e1339. Iosifidis Christos, Liu Jingshu, Gale Theodora, Ellingford Jamie M, Campbell Christopher, Ingram Stuart, Chandler Kate, Parry Neil R A, Black Graeme C, Sergouniotis Panagiotis |
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- Page last updated:Apr 22, 2024
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