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P29 Behr's syndrome is a mitochondrial disease due to autosomal recessive mutations in the C12orf65 gene

✍ Scribed by Pyle, A.; Venkateswaran, R.; Bartsakoulia, M.; Boczonadi, V.; Herczegfalvi, A.; Karcagi, V.; Lochmüller, H.; Taylor, R.; Chinnery, P.F.; Horvath, R.

Book ID: 122211346
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 55 KB
Volume: 24
Category: Article
ISSN: 0960-8966
DOI: 10.1016/S0960-8966(14)70045-8

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