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searching for RPGRIP1L 2 found (18 total)

alternate case: rPGRIP1L

Basal body (1,204 words) [view diff] exact match in snippet view article find links to article

Roepman, R. (2007). "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome". Nature Genetics

XPNPEP3 (1,011 words) [view diff] exact match in snippet view article find links to article

Othman, Mohammad I.; Waseem, Naushin (2009-06-01). "A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies". Nature Genetics