Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome

Title
Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome
Authors
Keywords
Chinese Family, Premature Ovarian Failure, Alanine Residue, Heterozygous Missense Mutation, Indel Mutation
Journal
BMC Medical Genetics
Volume 16, Issue 1, Pages -
Publisher
Springer Nature
Online
2015-08-31
DOI
10.1186/s12881-015-0217-7

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