7 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 34032273 | Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype. | 2022 Feb | 5 |
2 | 32630724 | A Novel Approach for the Identification of Pharmacogenetic Variants in MT-RNR1 through Next-Generation Sequencing Off-Target Data. | 2020 Jul 2 | 1 |
3 | 30523288 | The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence. | 2019 Mar | 3 |
4 | 27397648 | Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations. | 2016 Oct 10 | 1 |
5 | 26168747 | A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides? | 2015 Apr-Jun | 1 |
6 | 23969527 | Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects. | 2013 Oct | 1 |
7 | 20111055 | Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. | 2010 Mar | 1 |