Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation (Q35286584)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation |
scientific article |
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Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation (English)
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Malgorzata Krajewska-Walasek
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Thomas Gasser
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Tobias Haack
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Arcangela Iuso
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Thomas Klopstock
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Tim M Strom
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Katharina Heim
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Matthias Elstner
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Maja Hempel
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Monika B Hartig
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Sigrun Roeber
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Victoria Tarabin
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Wolfgang Mueller-Felber
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Hans Kretzschmar
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1 October 2011
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