SIMULTANEOUS MFN2 AND GDAP1 MUTATIONS CAUSE MAJOR MITOCHONDRIAL DEFECTS IN A PATIENT WITH CMT

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Veröffentlicht in:	Neurology 2011-04, Vol.76 (17), p.1524-1526
Hauptverfasser:	CASSEREAU, J, CASASNOVAS, C, PROCACCIO, V, CHEVROLLIER, A, GUEGUEN, N, MALINGE, M.-C, GUILLET, V, REYNIER, P, BONNEAU, D, AMATI-BONNEAU, P, BANCHS, I, VOLPINI, V
Format:	Artikel
Sprache:	eng
Schlagworte:	Aged Biological and medical sciences Charcot-Marie-Tooth Disease - complications Charcot-Marie-Tooth Disease - genetics Diseases of striated muscles. Neuromuscular diseases DNA Mutational Analysis Family Health Female GTP Phosphohydrolases Humans Life Sciences Male Medical sciences Membrane Proteins - genetics Middle Aged Mitochondrial Diseases - etiology Mitochondrial Diseases - genetics Mitochondrial Proteins - genetics Mutation - genetics Nerve Tissue Proteins - genetics Neurology
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