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Spectrum of somatic mitochondrial mutations in five cancers.
Larman TC, DePalma SR, Hadjipanayis AG; Cancer Genome Atlas Research Network; Protopopov A, Zhang J, Gabriel SB, Chin L, Seidman CE, Kucherlapati R, Seidman JG. Larman TC, et al. Among authors: seidman jg, seidman ce. Proc Natl Acad Sci U S A. 2012 Aug 28;109(35):14087-91. doi: 10.1073/pnas.1211502109. Epub 2012 Aug 13. Proc Natl Acad Sci U S A. 2012. PMID: 22891333 Free PMC article.
Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
Watkins H, Thierfelder L, Hwang DS, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.
Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
Solomon SD, Jarcho JA, McKenna W, Geisterfer-Lowrance A, Germain R, Salerni R, Seidman JG, Seidman CE. Solomon SD, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1990 Sep;86(3):993-9. doi: 10.1172/JCI114802. J Clin Invest. 1990. PMID: 1975599 Free PMC article.
514 results