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2015 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 25854
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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;173:117-124. doi: 10.1016/j.freeradbiomed.2021.07.029. Epub 2021 Jul 23.
Free Radic Biol Med. 2021.
PMID: 34303830
A Preliminary Genome-Wide Association Study of Acute Mountain Sickness Susceptibility in a Group of Nepalese Pilgrims Ascending to 4380 m.
MacInnis MJ, Widmer N, Timulsina U, Subedi A, Siwakoti A, Pandit BP, Freeman MG, Carter EA, Manokhina I, Thapa GB, Koehle MS.
MacInnis MJ, et al.
High Alt Med Biol. 2015 Dec;16(4):290-7. doi: 10.1089/ham.2015.0065. Epub 2015 Nov 24.
High Alt Med Biol. 2015.
PMID: 26600424
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