Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit.
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V. Kaplanová | V. Havlíčková | J. Houštěk | W. Sperl | J. Mayr | F. Zimmermann | J. Koch | P. Ješina | A. Pecinová | H. Nůsková | I. Magler