Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency

Lignende værker

• GLYCOSYLATION OF THE OCTN2 CARNITINE TRANSPORTER: STUDY OF NATURAL MUTATIONS IDENTIFIED IN PATIENTS WITH PRIMARY CARNITINE DEFICIENCY
  af: di San Filippo, Cristina Amat, et al.
  Udgivet: (2010)
• Primary Carnitine (OCTN2) Deficiency Without Neonatal Carnitine Deficiency
  af: de Boer, L., et al.
  Udgivet: (2012)
• Cholesterol stimulates the cellular uptake of L-carnitine by the carnitine/organic cation transporter novel 2 (OCTN2)
  af: Zhang, Lu, et al.
  Udgivet: (2021)
• Transport of butyryl-L-carnitine, a potential prodrug, via the carnitine transporter OCTN2 and the amino acid transporter ATB(0,+)
  af: Srinivas, Sonne R., et al.
  Udgivet: (2007)
• Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency
  af: Rasmussen, Jan, et al.
  Udgivet: (2014)