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Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: A novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality
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- Burwinkel B, Kreuder J, Schweitzer S, Vorgerd M, Gempel K, Gerbitz KD & Kilimann MW (author)
- Uppsala universitet,Institutionen för cell- och molekylärbiologi
- (creator_code:org_t)
- 1999
- 1999
- English.
- In: Biochem Biophys Res Commun. ; 261, s. 484-487
- Journal article (peer-reviewed)
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