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OCRL Deficiency Impairs Endolysosomal Function in a Humanized Mouse Model for Lowe Syndrome and Dent Disease
Festa, Beatrice Paola, Berquez, Marine, Gassama, Alkaly, Amrein, Irmgard, Ismail, Hesham M, Samardzija, Marijana, Staiano, Leopoldo, Luciani, Alessandro, Grimm, Christian, Nussbaum, Robert L, De MatteLanguage:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddy449
Date:
December, 2018
File:
PDF, 2.16 MB
english, 2018