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Wiley, Human Mutation: Variation, Informatics and Disease, 4(34), p. 655-655, 2013

DOI: 10.1002/humu.22286

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Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation

This paper is available in a repository.
This paper is available in a repository.

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