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Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects
Gaboon, Nagwa E.A., Banaganapalli, Babajan, Nasser, Khalidah, Razeeth, Mohammed, Alsaedi, Mosab S., Rashidi, Omran M., Abdelwehab, Lereen S., Alahmadi, Turki Saad, Safdar, Osama Y., Shaik, Jilani, ChoLanguage:
english
Journal:
Saudi Journal of Biological Sciences
DOI:
10.1016/j.sjbs.2019.10.001
Date:
October, 2019
File:
PDF, 2.97 MB
english, 2019