Associated Papers
Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations.
Zou G et al.
Molecular Vision, 2021
Next-generation genetic testing for retinitis pigmentosa.
Neveling K et al.
Human Mutation, 2012
22334370 (PubMed )
Supplement: humu0033-0963-sd1.pdf
RPGRIP1 is mutated in Leber congenital amaurosis: a mini-review.
Koenekoop RK
Ophthalmic Genetics, 2005
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