← Evidence map

ArticleHuman molecular genetics2021

A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect.

Susanne Kohl et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

2 papers cite it

2021
2022
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 33891002