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MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome
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- Naess, K (author)
- Karolinska Institutet
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- Freyer, C (author)
- Karolinska Institutet
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- Bruhn, H (author)
- Karolinska Institutet
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- Dobeln, U (author)
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- (creator_code:org_t)
- Elsevier BV, 2009
- 2009
- English.
- In: Biochimica et biophysica acta. - : Elsevier BV. - 0006-3002 .- 0005-2728. ; 1787:5, s. 484-490
- Journal article (peer-reviewed)
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- Naess, K
- Freyer, C
- Bruhn, H
- Wibom, R
- Malm, G
- Nennesmo, I
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- Dobeln, U
- Larsson, NG
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