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de Aguiar Pastore Silva J, Emilia de Souza Fabre M, Waitzberg DL
Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter
Guerreiro G, Mescka CP, Sitta A et al (2015) Urinary biomarkers of oxidative damage in maple syrup urine disease: the l-carnitine role
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Chromium Picolinate con L-Carnitina
