Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa
European Journal of Ophthalmology, 07/06/2012
Ksantini M et al. – MERTK mutations lead to severe retinitis pigmentosa with discrete dot–like autofluorescent deposits at early stages, which are a hallmark of this MERTK–specific dystrophy.



