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Burwinkel B, Kreuder J, Schweitzer S, Vorgerd M, Gempel K, Gerbitz KD, Kilimann MW: Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality

doi: 10.1111/j.1085-9489.2006.00066.x [DOI] [PubMed] [Google Scholar] 32.Scarpini E, Sacilotto G, Baron P, et al

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