Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 e subunit

MAYR, J. A., HAVLÍČKOVÁ, V., ZIMMERMANN, F., MAGLER, I., KAPLANOVÁ, V., JEŠINA, P., PECINOVÁ, A., NŮSKOVÁ, H., KOCH, J., SPERL, W., HOUŠTĚK, J. Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 e subunit. Human Molecular Genetics. 2010, 19(17), 3430-3439. ISSN 0964-6906. E-ISSN 1460-2083. Dostupné z: doi: 10.1093/hmg/ddq254