eyes absent homolog 1 isoform 4 [Homo sapiens]

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[Clinical phenotypic and genetic analysis of syndrome families with EYA1 gene variants]. [Lin Chuang Er Bi Yan Hou Tou J...]
[Clinical phenotypic and genetic analysis of syndrome families with EYA1 gene variants].
Shao H, Li Y, Zhao H, Lin K, Gao Y, Ming C, Ma J. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 Jul; 38(7):636-640.
Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms. [BMC Med Genomics. 2024]
Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms.
Zhang H, Gao J, Wang H, Liu M, Lu S, Xu H, Tang W, Zheng G. BMC Med Genomics. 2024 Apr 16; 17(1):89. Epub 2024 Apr 16.
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family. [Mol Genet Genomic Med. 2022]
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family.
Yalcouyé A, Traoré O, Diarra S, Schrauwen I, Esoh K, Kadlubowska MK, Bharadwaj T, Adadey SM, Kéita M, Guinto CO, et al. Mol Genet Genomic Med. 2022 Jul; 10(7):e1995. Epub 2022 Jun 14.

RefSeq genomic sequence
See the genomic reference sequence for the EYA1 gene (NG_011735.4).
RefSeq mRNA
See reference mRNA sequence for the EYA1 gene (NM_001288574.2).
RefSeq protein isoforms
See 43 reference sequence protein isoforms for the EYA1 gene.

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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
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OncoMX cancer biomarker resource
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reagents [ExactAntigen/Labome]
reagents
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