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TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways
Dorval, Guillaume, Kuzmuk, Valeryia, Gribouval, Olivier, Welsh, Gavin I., Bierzynska, Agnieszka, Schmitt, Alain, Miserey-Lenkei, Stéphanie, Koziell, Ania, Haq, Shuman, Benmerah, Alexandre, Mollet, GérLanguage:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2018.12.016
Date:
January, 2019
File:
PDF, 2.00 MB
english, 2019