Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: Disease and HARS2[original query] |
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| Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis. European journal of human genetics : EJHG 2015 Aug . Kinnersley Ben, Kamatani Yoichiro, Labussière Marianne, Wang Yufei, Galan Pilar, Mokhtari Karima, Delattre Jean-Yves, Gousias Konstantinos, Schramm Johannes, Schoemaker Minouk J, Swerdlow Anthony, Fleming Sarah J, Herms Stefan, Heilmann Stefanie, Nöthen Markus M, Simon Matthias, Sanson Marc, Lathrop Mark, Houlston Richard |
| Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA Synthetases. Genes 2024 7 15 (7): . María Domínguez-Ruiz, Margarita Olarte, Esther Onecha, Irene García-Vaquero, Nancy Gelvez, Greizy López, Manuela Villamar, Matías Morín, Miguel A Moreno-Pelayo, Carmelo Morales-Angulo, Rubén Polo, Martha L Tamayo, Ignacio Del Castil |
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