Suchergebnisse - "Steffann, J"

PubPharm (2)

1

A constant and similar assembly defect of mitochondrial respiratory chain complex I allows rapid identification of NDUFS4 mutations in patients with Leigh syndrome

enthalten in: Biochimica et biophysica acta | 2012

von Assouline, Z. | Jambou, M. | Rio, M. | +11

2

A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency

enthalten in: Journal of medical genetics | 2011

von Lebre, A. | Rio, M. | Faivre d'Arcier, L. | +23

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