Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: Hearing Loss and LARS2[original query] |
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| A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family. Journal of clinical research in pediatric endocrinology 2016 Apr . Dursun Fatma, Mohamoud Hussein Sheikh Ali, Karim Noreen, Naeem Muhammad, Jelani Musharraf, K?rm?z?bekmez Hev |
| 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 |
- Page last reviewed:Feb 1, 2024
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