Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: MAB21L1[original query] |
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Identification of missense MAB21L1 variants in microphthalmia and aniridia. Human mutation 2021 5 42 (7): 877-890. Seese Sarah E, Reis Linda M, Deml Brett, Griffith Christopher, Reich Adi, Jamieson Robyn V, Semina Elena |
Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD Syndrome. Investigative ophthalmology & visual science 2023 3 64 (3): 19. Wang Panfeng, Wu Pengsen, Wang Junwen, Zeng Yiyan, Jiang Yi, Wang Yingwei, Li Shiqiang, Xiao Xueshan, Zhang Qingjio |
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- Page last updated:Mar 25, 2024
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