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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Disease and MTRNR2L2[original query]
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. GWAS Catalog
The Lancet. Neurology 2017 Jun .
Moss Davina J Hensman, Pardiñas Antonio F, Langbehn Douglas, Lo Kitty, Leavitt Blair R, Roos Raymund, Durr Alexandra, Mead Simon, , , Holmans Peter, Jones Lesley, Tabrizi Sarah
Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease.
BMC research notes 2019 Nov 12 (1): 759.
Eltermaa Mall, Jakobson Maili, Utt Meeme, Kõks Sulev, Mägi Reedik, Starkopf Jo
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