martes, 29 de septiembre de 2020

Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) | Mutagenesis | Oxford Academic

Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) | Mutagenesis | Oxford Academic

Issue Cover

Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) 

Mutagenesis, Volume 26, Issue 2, March 2011, Pages 283–289, https://doi.org/10.1093/mutage/geq086

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