Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia.

Habibi, Imen

Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia. [electronic resource] - Advances in experimental medicine and biology 2019 - 221-226 p. digital

Publication Type: Journal Article

0065-2598

10.1007/978-3-030-27378-1_36 doi


Anophthalmos--genetics
Egypt
Forkhead Transcription Factors--genetics
Frameshift Mutation
Homeodomain Proteins--genetics
Humans
Microphthalmos--genetics
Mutation
Phenotype
SOXB1 Transcription Factors--genetics
Sequence Deletion
Transcription Factors--genetics