Citations for
1AMS1, MNGIE2, PEO1, PNDC, POLG, SANDO
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.
Hum Mutat 29(9):E150-E172. [Epub ahead of print] 2008
2MNGIE2, POLG
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.
Van Goethem G, Schwartz M, Löfgren A, Dermaut B, Van Broeckhoven C, Vissing J.
Eur J Hum Genet 11(7):547-9. 2003
3MNGIE2
Multiple mtDNA deletions with features of MNGIE.
Vissing J, Ravn K, Danielsen ER, Dunø M, Wibrand F, Wevers RA, Schwartz M.
Neurology 59(6):926-9. 2002