l acetyl carnitine ph degrade Role of in disease | Nutrition & Metabolism Exploring the potential anti-thyroid activity
Description
Abstract Background: Systemic primary carnitine deficiency is an autosomal recessive disorder of the carnitine cycle caused by mutations in the SLC22A5 gene that encodes the carnitine transporter, organic cation transporter
Cederbaum SD, Koo-McCoy S, Tein I, Hsu BY, Ganguly A, Vilain E, Dipple K, Cvitanovic-Sojat L, Stanley C: Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency
doi: 10.1016/j.mce.2010.05.019
Este produto no deve ser utilizado no caso de hipersensibilidade ou alergia a qualquer um dos seus constituintes
