Tosetto, Addis, Caridi et al.: "Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations." in: Pediatric nephrology (Berlin, Germany), Vol. 24, Issue 10, pp. 1967-73, 2009 (PubMed).
Coon, Mukherjee, Hanna et al.: "Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase." in: Human molecular genetics, Vol. 18, Issue 23, pp. 4478-91, 2009 (PubMed).
Cui, Guerriero, Szalinski et al.: "OCRL1 function in renal epithelial membrane traffic." in: American journal of physiology. Renal physiology, Vol. 298, Issue 2, pp. F335-45, 2010 (PubMed).
Coutton, Monnier, Rendu et al.: "Development of a multiplex ligation-dependent probe amplification (MLPA) assay for quantification of the OCRL1 gene." in: Clinical biochemistry, Vol. 43, Issue 6, pp. 609-14, 2010 (PubMed).
Swan, Tomasini, Pirruccello et al.: "Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 8, pp. 3511-6, 2010 (PubMed).