A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
Khanna H; Davis EE; Murga-Zamalloa CA; Estrada-Cuzcano A; Lopez I; den Hollander AI; Zonneveld MN; Othman MI; Waseem N; Chakarova CF; Maubaret C; Diaz-Font A; MacDonald I; Muzny DM; Wheeler DA; Morgan M; Lewis LR; Logan CV; Tan PL; Beer MA; Inglehearn CF; Lewis RA; Jacobson SG; Bergmann C; Beales PL; Attié-Bitach T; Johnson CA; Otto EA; Bhattacharya SS; Hildebrandt F; Gibbs RA; Koenekoop RK; Swaroop A; Katsanis N; Nature Genetics, 2009, vol. 41, issue 6, p 739, ISSN 15461718. ISBN 15461718.

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