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 MatteМова:
english
Журнал:
Human Molecular Genetics
DOI:
10.1093/hmg/ddy449
Date:
December, 2018
Файл:
PDF, 2.16 MB
english, 2018