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A catalytic defect in mitochondrial respiratory chain complex I due to a mutation in NDUFS2 in a patient with Leigh syndrome

✍ Scribed by Lock Hock Ngu; Leo G. Nijtmans; Felix Distelmaier; Hanka Venselaar; Sjenet E. van Emst-de Vries; Mariël A.M. van den Brand; Berendien J.M. Stoltenborg; Liesbeth T. Wintjes; Peter H. Willems; Lambertus P. van den Heuvel; Jan A. Smeitink; Richard J.T. Rodenburg

Book ID: 116271062
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 867 KB
Volume: 1822
Category: Article
ISSN: 0925-4439
DOI: 10.1016/j.bbadis.2011.10.012

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