MITOMAP References for 3308 T-G

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Index	PMID	Date	Reference
1	11820805	2002	Vives-Bauza, C., Andreu, A. L., Manfredi, G., Beal, M. F., Janetzky, B., Gruenewald, T. H., Lin, M. T. (2002) Sequence analysis of the entire mitochondrial genome in Parkinson's disease Biochemical and Biophysical Research Communications . 290 (5): 1593-1601 .
2	15466077	2004	Opdal, S. H., Rognum, T. O. (2004) The sudden infant death syndrome gene: does it exist? Pediatrics . 114 (4): e506-512 .
3	NA	2014	van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb .
4	37777527	2023	Hong, Y. S., Battle, S. L., Shi, W., Puiu, D., Pillalamarri, V., Xie, J., Pankratz, N., Lake, N. J., Lek, M., Rotter, J. I., Rich, S. S., Kooperberg, C., Reiner, A. P., Auer, P. L., Heard-Costa, N., Liu, C., Lai, M., Murabito, J. M., Levy, D., Grove, M. L., Alonso, A., Gibbs, R., Dugan-Perez, S., Gondek, L. P., Guallar, E., Arking, D. E. (2023) Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality Nature Communications . 14 (1): 6113 .