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[DOI] [PubMed] [Google Scholar] 85.Iqbal I., Wilairatana P., Saqib F., Nasir B., Wahid M., Latif M.F., Iqbal A., Naz R., Mubarak M.S
Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy
M., Senes, M., Tekeli, N., and Yucel, D
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