Varaico: Literature-Extracted Genetic Variants

Gene:MERTK
Variant:p.R20T
Back to variants list

MERTK

NM_006343.3:p.R20T

Associated Papers

MERTK mutation update in inherited retinal diseases.

Audo I et al.

Human Mutation, 2018

A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.

Jinda W et al.

Molecular Vision, 2016

Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene.

Tschernutter M et al.

The British Journal of Ophthalmology, 2006

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."