Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation-Reference-Cited by-同舟云学术

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Published:2011-10 Issue:4 Volume:89 Page:543-550
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hartig Monika B.,Iuso Arcangela,Haack Tobias,Kmiec Tomasz,Jurkiewicz Elzbieta,Heim Katharina,Roeber Sigrun,Tarabin Victoria,Dusi Sabrina,Krajewska-Walasek Malgorzata,Jozwiak Sergiusz,Hempel Maja,Winkelmann Juliane,Elstner Matthias,Oexle Konrad,Klopstock Thomas,Mueller-Felber Wolfgang,Gasser Thomas,Trenkwalder Claudia,Tiranti Valeria,Kretzschmar Hans,Schmitz Gerd,Strom Tim M.,Meitinger Thomas,Prokisch Holger

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference15 articles.

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