Homo sapiens forkhead box L2 (FOXL2), RefSeqGene (LRG_1295) on chromos - Nucleotide

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Deletion of cis-regulatory Element in FOXL2 Promoter in a Chinese Family of Type II Blepharophimosis-ptosis-epicanthus Inversus Syndrome with Polydactyly. [J Craniofac Surg. 2024]
Deletion of cis-regulatory Element in FOXL2 Promoter in a Chinese Family of Type II Blepharophimosis-ptosis-epicanthus Inversus Syndrome with Polydactyly.
Shen Q, Zhao X, Ji Y, Chai P. J Craniofac Surg. 2024 Jan-Feb 01; 35(1):e52-e56. Epub 2023 Nov 8.
Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family. [BMC Ophthalmol. 2023]
Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family.
Lin ZB, Chen ZJ, Yang H, Ding XR, Li J, Pan AP, Sun HS, Yu AY, Chen SH. BMC Ophthalmol. 2023 Nov 7; 23(1):446. Epub 2023 Nov 7.
FOXL2: a gene central to ovarian function. [J Clin Pathol. 2023]
FOXL2: a gene central to ovarian function.
Mubeen A, Parra-Herran C. J Clin Pathol. 2023 Dec; 76(12):798-801. Epub 2023 Oct 5.

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Protein sequence from Nucleotide coding region
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Nucleotide