OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease

MLA

UCL - SSS/IREC/NEFR - Pôle de Néphrologie, et al. “OCRL Deficiency Impairs Endolysosomal Function in a Humanized Mouse Model for Lowe Syndrome and Dent Disease.” Human Molecular Genetics, Vol. 28, No.12, p. 1931-1946 (2018), 2018. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1288277868&authtype=sso&custid=ns315887.

APA

UCL - SSS/IREC/NEFR - Pôle de Néphrologie, Festa, B. P., Berquez, M., Gassama, A., Amrein, I., Ismail, H. M., Samardzija, M., Staiano, L., Luciani, A., Grimm, C., Nussbaum, R. L., De Matteis, M. A., Dorchies, O. M., Scapozza, L., Wolfer, D. P., & Devuyst, O. (2018). OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease. Human Molecular Genetics, Vol. 28, No.12, p. 1931-1946 (2018).

Chicago

UCL - SSS/IREC/NEFR - Pôle de Néphrologie, Beatrice Paola Festa, Marine Berquez, Alkaly Gassama, Irmgard Amrein, Hesham M Ismail, Marijana Samardzija, et al. 2018. “OCRL Deficiency Impairs Endolysosomal Function in a Humanized Mouse Model for Lowe Syndrome and Dent Disease.” Human Molecular Genetics, Vol. 28, No.12, p. 1931-1946 (2018). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1288277868&authtype=sso&custid=ns315887.