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Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ.
Barel O, Shorer Z, Flusser H, Ofir R, Narkis G, Finer G, Shalev H, Nasasra A, Saada A, Birk OS. Barel O, et al. Among authors: Finer G. Am J Hum Genet. 2008 May;82(5):1211-6. doi: 10.1016/j.ajhg.2008.03.020. Epub 2008 Apr 24. Am J Hum Genet. 2008. PMID: 18439546 Free PMC article.
Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9.
Barel O, Shalev SA, Ofir R, Cohen A, Zlotogora J, Shorer Z, Mazor G, Finer G, Khateeb S, Zilberberg N, Birk OS. Barel O, et al. Among authors: Finer G. Am J Hum Genet. 2008 Aug;83(2):193-9. doi: 10.1016/j.ajhg.2008.07.010. Am J Hum Genet. 2008. PMID: 18678320 Free PMC article.
A conceptual framework for the molecular pathogenesis of progressive kidney disease.
Schnaper HW, Hubchak SC, Runyan CE, Browne JA, Finer G, Liu X, Hayashida T. Schnaper HW, et al. Among authors: Finer G. Pediatr Nephrol. 2010 Nov;25(11):2223-30. doi: 10.1007/s00467-010-1503-4. Epub 2010 Mar 30. Pediatr Nephrol. 2010. PMID: 20352456 Free PMC article. Review.
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