Corrigendum: Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome
- Resource Type
- article
- Source
- Frontiers in Genetics, Vol 15 (2024)
- Subject
blepharophimosis-ptosis-epicanthus inversus syndrome FOXL2 variant whole exome sequencing tansfection protein model prediction Genetics QH426-470 - Language
- English
- ISSN
- 1664-8021