Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy.

Kondo, Hiroyuki

Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy. [electronic resource] - Ophthalmic genetics 12 2016 - 462-464 p. digital

Publication Type: Letter; Research Support, Non-U.S. Gov't

1744-5094

10.3109/13816810.2015.1120316 doi


Base Sequence
Basic Helix-Loop-Helix Transcription Factors--genetics
Child
DNA Mutational Analysis
Eye Diseases, Hereditary
Familial Exudative Vitreoretinopathies
Female
Homozygote
Humans
Infant
Male
Molecular Sequence Data
Mutation
Retinal Diseases--congenital
Sequence Deletion