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Txn1 mutation is a monogenic cause of chronic kidney dise... | ResearchHub
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Txn1 mutation is a monogenic cause of chronic kidney disease associated with mitochondrial dysfunction in rats
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Authors
Iori Ohmori
6 more
Iori Ohmori
•
Mamoru Ouchida
4 more
•
Tomoji Mashimo
Published
August 15, 2023
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Topics
Biology
Physiology
Medicine
Internal Medicine
Endocrinology
Show all topics
DOI
10.1101/2023.08.14.553187
License
CC-BY-NC-ND
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PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Physiology
Medicine
Internal Medicine
Endocrinology
Show all topics
DOI
10.1101/2023.08.14.553187
License
CC-BY-NC-ND
Other Formats
PDF
