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Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies

✍ Scribed by Saskia J.G. Hoefs; Ola H. Skjeldal; Richard J. Rodenburg; Bård Nedregaard; Edwin P.M. van Kaauwen; Ute Spiekerkötter; Jürgen-Christoph von Kleist-Retzow; Jan A.M. Smeitink; Leo G. Nijtmans; Lambert P. van den Heuvel

Book ID: 116988984
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 481 KB
Volume: 100
Category: Article
ISSN: 1096-7192
DOI: 10.1016/j.ymgme.2010.03.015

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