Absence of an Orphan Mitochondrial Protein, C19orf12,...

The American Journal of Human Genetics 2011 Vol. 89; Iss. 4

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

Monika B. Hartig, Arcangela Iuso, Tobias Haack, Tomasz Kmiec, Elzbieta Jurkiewicz, Katharina Heim, Sigrun Roeber, Victoria Tarabin, Sabrina Dusi, Malgorzata Krajewska-Walasek, Sergiusz Jozwiak, Maja H
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Volume:
89
Year:
2011
Language:
english
Pages:
8
DOI:
10.1016/j.ajhg.2011.09.007
File:
PDF, 899 KB
english, 2011
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