Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis.
Wolf MT; Saunier S; O'Toole JF; Wanner N; Groshong T; Attanasio M; Salomon R; Stallmach T; Sayer JA; Waldherr R; Griebel M; Oh J; Neuhaus TJ; Josefiak U; Antignac C; Otto EA; Hildebrandt F; Kidney International, 2007, vol. 72, issue 12, p 1520, ISSN 00852538. ISBN 00852538.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef