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Description
Carnitine supplementation for preterm infants with recurrent apnea
Cell Metab 27:4256
Primary carnitine deficiency or carnitine transporter defect is an autosomal recessive disorder of fatty acid oxidation caused by heterozygous mutations in the SLC22A5 gene that encodes the high-affinity carnitine transporter, OCTN2
Non sono disponibili studi clinici con la somministrazione della vitamina B12 o questo medicinale in donne in gravidanza
Zusammen mit Vitamin C entsteht aus Prolin Hydroxyprolin, ein wichtiger Bestandteil von Kollagen und Elastin
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