Genomic Disruption of FOXL2 in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Type 2
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference12 articles.
1. Functional analysis of a novel FOXL2 indel mutation in Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome type I;Chai;Int J Biol Sci,2017
2. Structure, evolution and expression of the FOXL2 transcription unit;Cocquet;Cytogenet Genome Res,2003
3. Evolution and expression of FOXL2;Cocquet;J Med Genet,2002
4. The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome;Crisponi;Nat Genet,2001
5. FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation;De Baere;Am J Hum Genet,2003
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Evaluation of the clinical effect of 4D digital strabismus and amblyopia visual function correction system combined with traditional comprehensive treatment methods on anisometropic amblyopia;2024-05-30
2. The Genetic and Clinical Features of FOXL2-Related Blepharophimosis, Ptosis and Epicanthus Inversus Syndrome;Genes;2021-03-04
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