Open access
Jul 2026
XXYLT1 and Mendelian Retinal Dystrophy
Findings support the need to include XXYLT1 in clinical IRD gene panels, one of the identified genes, as a rare mendelian IRD gene in independent Finnish and UK clinical cohorts.
Minna Kraatari-Tiri, Hina Ishtiaq, J. Tyrmi et al.
· JAMA ophthalmology · 0 citations