Author:
Huddart Rachel,Altman Russ
Publisher
Springer Nature Singapore
Reference73 articles.
1. McInnes G, Lavertu A, Sangkuhl K, Klein TE, Whirl-Carrillo M, Altman RB (2021) Pharmacogenetics at scale: an analysis of the UK Biobank. Clin Pharmacol Ther 109(6):1528–1537
2. Whirl-Carrillo M, Huddart R, Gong L, Sangkuhl K, Thorn CF, Whaley R et al (2021) An evidence-based framework for evaluating pharmacogenomics knowledge for personalized medicine. Clin Pharmacol Ther 110(3):563–572
3. Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ et al (1993) Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 4(3):289–294
4. Thyagarajan D, Bressman S, Bruno C, Przedborski S, Shanske S, Lynch T et al (2000) A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy. Ann Neurol 48(5):730–736
5. Wu L, Li R, Chen J, Chen Y, Yang M, Wu Q (2018) Analysis of mitochondrial A1555G mutation in infants with hearing impairment. Exp Ther Med 15(6):5307–5313