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P4.60 Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation

✍ Scribed by H.A.L. Tuppen; J. Fehmi; B. Czermin; P. Goffrini; F. Meloni; I. Ferrero; L. He; E.L. Blakely; R. McFarland; R. Horvath; D.M. Turnbull; R.W. Taylor

Book ID: 116794685
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 40 KB
Volume: 20
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2010.07.256

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