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Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation.

Klinische Padiatrie - 1 Jul 2022

Yildiz Damla, Yazici Mutlu Uysal, Oguz Melahat Melek, Torun Emine Gulsah, Sezer Abdullah, Kiliç Mustafa

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PMID: 35820418
DOI: 10.1055/a-1730-5472

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