reference/9546885

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9546885

Outgoing Links

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endingPage	124
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publicationName	Free Radical Biology and Medicine
startingPage	117
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bibliographicCitation	Zhang J, Dai Y, Wu D, Li Y, Xu J. Whole exome sequencing identified FAM149A as a plausible causative gene for congenital hereditary endothelial dystrophy, affecting Nrf2-Antioxidant signaling upon oxidative stress. Free Radic Biol Med. 2021 Sep;173():117–24. doi: 10.1016/j.freeradbiomed.2021.07.029. PMID: 34303830.
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date	202109
identifier	https://doi.org/10.1016/j.freeradbiomed.2021.07.029 https://pubmed.ncbi.nlm.nih.gov/34303830
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Whole exome sequencing identified FAM149A as a plausible causative gene for congenital hereditary endothelial dystrophy, affecting Nrf2-Antioxidant signaling upon oxidative stress
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