Article
Screening of a large PAX6 cohort identified many novel variants and emphasises the importance of the paired and homeobox domains.
European journal of medical genetics - 1 Jul 2020
Cross Esther, Duncan-Flavell Philippa J, Howarth Rachel J, Crooks Richard O, Thomas N Simon, Bunyan David J
Abstract excerpt
Pathogenic variants within PAX6 are most often associated with aniridia, but have been linked with other phenotypes such as nystagmus, cataracts and foveal hypoplasia. Data are presented from a large cohort of 434 probands referred for PAX6 diagnostic testing. This analysis identified a wide range of pathogenic variants (n = 145) in 254 probands (including 61 novel variants). Excluding missense variants predicted...
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