Homo sapiens MAB21L1 mRNA for protein mab-21-like 1, complete cds, clo - Nucleotide

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External genitalia phenotypes of a Mab21l1-null mouse model for cerebellar, ocular, craniofacial, and genital (COFG) syndrome. [Anat Rec (Hoboken). 2024]
External genitalia phenotypes of a Mab21l1-null mouse model for cerebellar, ocular, craniofacial, and genital (COFG) syndrome.
Promsut W, Yamada R, Takami S, Miyazaki N, Uemura M, Hiramatsu R, Takahashi N, Kanai Y. Anat Rec (Hoboken). 2024 May; 307(5):1943-1959. Epub 2023 Sep 26.
Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD Syndrome. [Invest Ophthalmol Vis Sci. 2023]
Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD Syndrome.
Wang P, Wu P, Wang J, Zeng Y, Jiang Y, Wang Y, Li S, Xiao X, Zhang Q. Invest Ophthalmol Vis Sci. 2023 Mar 1; 64(3):19.
Single amino acid variation in MAB21L1 is dominantly associated with congenital eye defects. [J Med Genet. 2023]
Single amino acid variation in MAB21L1 is dominantly associated with congenital eye defects.
Meng F, Li X, Zhang J, Gao Z, Yang X, Liu Z, Liu Y, Guo T, Wang L, Yang L, et al. J Med Genet. 2023 Jul; 60(7):655-661. Epub 2022 Nov 29.

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Nucleotide