Homozygous Mutation in MERTK Causes Severe Autosomal Recessive Retinitis Pigmentosa

Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family

(2010) A. Shahzadi et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

The Retinal Pigment Epithelium in Health and Disease

(2010) J. R. Sparrrow et al.   CURRENT MOLECULAR MEDICINE

Tubby and tubby-like protein 1 are new MerTK ligands for phagocytosis

(2010) Nora B Caberoy et al.   EMBO JOURNAL

Characterisation of severe rod-cone dystrophy in a consanguineous family with a splice site mutation in the MERTK gene

(2009) P Charbel Issa et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa

(2008) A J Brea-Fernandez et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Leber congenital amaurosis: Genes, proteins and disease mechanisms

(2008) Anneke I. den Hollander et al.   PROGRESS IN RETINAL AND EYE RESEARCH