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    Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect

    Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect by Hatice Mutlu-Albayrak, Judit Bene, Mehmet Burhan Oflaz, Tijen Tanyalçın, Hüseyin Çaksen, Bela Melegh

    Published 2015-01-01
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