Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency-Reference-Cited by-同舟云学术

Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency

Published:2014-09 Issue:3 Volume:95 Page:315-325
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Melchionda Laura,Haack Tobias B.,Hardy Steven,Abbink Truus E.M.,Fernandez-Vizarra Erika,Lamantea Eleonora,Marchet Silvia,Morandi Lucia,Moggio Maurizio,Carrozzo Rosalba,Torraco Alessandra,Diodato Daria,Strom Tim M.,Meitinger Thomas,Tekturk Pinar,Yapici Zuhal,Al-Murshedi Fathiya,Stevens René,Rodenburg Richard J.,Lamperti Costanza,Ardissone Anna,Moroni Isabella,Uziel Graziella,Prokisch Holger,Taylor Robert W.,Bertini Enrico,van der Knaap Marjo S.,Ghezzi Daniele,Zeviani Massimo

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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