A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia
by Szklarczyk, Radek (Author)
, Wanschers, Bas F. J. (Author)
, Nijtmans, Leo G. (Author)
, Rodenburg, Richard J. (Author)
, Zschocke, Johannes (Author)
, Dikow, Nicola (Author)
, van den Brand, Mariël A. M. (Author)
, Hendriks-Franssen, Marthe G. M. (Author)
, Gilissen, Christian (Author)
, Veltman, Joris A. (Author)
, Nooteboom, Marco (Author)
, Koopman, Werner J. H. (Author)
, Willems, Peter H.G.M. (Author)
, Smeitink, Jan A. M. (Author)
, Huynen, Martijn A. (Author)
, van den Heuvel, Lambertus P. (Author)
,
Call Number:
Loading…
Located:
Loading…
Article (Journal)
Online Resource