Novel causative variants in patients with achromatopsia.

CONCLUSIONS: These novel variants expand the genotypes associated with ACHM and may help in future therapy development for ACHM.
PMID: 30289319 [PubMed - as supplied by publisher]

Source: Ophthalmic Genetics - October 6, 2018 Category: Opthalmology Tags: Ophthalmic Genet Source Type: research