期刊
HUMAN MOLECULAR GENETICS
卷 28, 期 R1, 页码 R42-R48出版社
OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddz140
关键词
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资金
- European Research Council (IEMTx)
- Fondazione Telethon, Italy [TCBP37TELC, TCBMT3TELD]
- Rashid Family Fund
Urea cycle disorders (UCD) are inborn errors of metabolism caused by deficiency of enzymes required to transfer nitrogen from ammonia into urea. Current paradigms of treatment focus on dietary manipulations, ammonia scavenger drugs, and orthotopic liver transplantation. In the last years, there has been intense preclinical research aiming at developing more effective treatments for UCD, and as a result, several novel approaches based on new knowledge of the disease pathogenesis, cell and gene therapies are currently under clinical investigation. We provide an overview of the latest advances for the development of novel therapies for UCD.
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