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

✍ Scribed by Helen A.L. Tuppen; Janev Fehmi; Birgit Czermin; Paola Goffrini; Francesca Meloni; Iliana Ferrero; Langping He; Emma L. Blakely; Robert McFarland; Rita Horvath; Douglass M. Turnbull; Robert W. Taylor

Book ID: 116988999
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 366 KB
Volume: 100
Category: Article
ISSN: 1096-7192
DOI: 10.1016/j.ymgme.2010.04.010

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