Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects - Concepedia

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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

DOI Full Paper Access

18

Citations

14

References

2019

Year

Nagwa E. A. Gaboon, Babajan Banaganapalli, Khalidah Khalid Nasser, Mohammed Razeeth Shait Mohammed, Mosab S. Alsaedi, Omran M. Rashidi, Lereen S. Abdelwehab, Turki S Alahmadi, Osama Safdar, Jilani Shaik,

Saudi Journal of Biological Sciences

References

	Year	Citations

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