Košík

0076247 - FGÚ 2007 NL eng A - Abstrakt
Mayr, J. A. - Koch, J. - Kurnik, P. - Pecina, Petr - Houštěk, Josef - Sperl, W.
Severe peripheral neuropathy in a patient with 3-methylglutaconic aciduria and F1F0-ATP synthase deficiency of nuclear genetic origin.
[Periferní neuropatie u pacienta s 3-metylglutaconovou acidurií a deficiencí F1Fo-ATP syntázy jaderného původu.]
Journal of Inherited Metabolic Disease. Roč. 29, S1 (2006), s. 118-118. ISSN 0141-8955. E-ISSN 1573-2665.
[International Congress of Inborn Errors of Metabolism /10./. 12.09.2006-16.09.2006, Chiba]
Klíčová slova: ATP synthase * mitochondria
Kód oboru RIV: CE - Biochemie
Trvalý link: http://hdl.handle.net/11104/0143399