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Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
Wong LJ, Naviaux RK, Brunetti-Pierri N, Zhang Q, Schmitt ES, Truong C, Milone M, Cohen BH, Wical B, Ganesh J, Basinger AA, Burton BK, Swoboda K, Gilbert DL, Vanderver A, Saneto RP, Maranda B, Arnold G, Abdenur JE, Waters PJ, Copeland WC. Wong LJ, et al. Hum Mutat. 2008 Sep;29(9):E150-72. doi: 10.1002/humu.20824. Hum Mutat. 2008. PMID: 18546365 Free PMC article.
De novo mutations in POLG presenting with acute liver failure or encephalopathy.
Lutz RE, Dimmock D, Schmitt ES, Zhang Q, Tang LY, Reyes C, Truemper E, McComb RD, Hernandez A, Basinger A, Wong LJ. Lutz RE, et al. Among authors: wong lj. J Pediatr Gastroenterol Nutr. 2009 Jul;49(1):126-9. doi: 10.1097/MPG.0b013e31817d9cad. J Pediatr Gastroenterol Nutr. 2009. PMID: 19252446 No abstract available.
376 results