myelin transcription factor 1-like protein isoform X1 [Homo sapiens]

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2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review. [Eur J Hum Genet. 2023]
2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review.
Bouassida M, Egloff M, Levy J, Chatron N, Bernardini L, Le Guyader G, Tabet AC, Schluth-Bolard C, Brancati F, Giuffrida MG, et al. Eur J Hum Genet. 2023 Aug; 31(8):895-904. Epub 2023 May 15.
MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects. [Hum Genet. 2022]
MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.
Coursimault J, Guerrot AM, Morrow MM, Schramm C, Zamora FM, Shanmugham A, Liu S, Zou F, Bilan F, Le Guyader G, et al. Hum Genet. 2022 Jan; 141(1):65-80. Epub 2021 Nov 8.
A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study. [Sci Rep. 2021]
A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study.
Yoshimura K, Morita Y, Konomi K, Ishida S, Fujiwara D, Kobayashi K, Tanaka M. Sci Rep. 2021 May 3; 11(1):9446. Epub 2021 May 3.

RefSeq genomic sequence
See the genomic reference sequence for the MYT1L gene (NG_051313.1).
RefSeq protein isoforms
See 56 reference sequence protein isoforms for the MYT1L gene.

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Protein