putative nucleotidyltransferase MAB21L1 [Bos taurus]

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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.
Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB21L1. [Sci Rep. 2016]
Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB21L1.
de Oliveira Mann CC, Kiefersauer R, Witte G, Hopfner KP. Sci Rep. 2016 Jun 8; 6:27498. Epub 2016 Jun 8.

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