Twin Brothers with Carnitine Membrane Transporter Deficiency: A Case Study

Carnitine membrane transporter deficiency or primary carnitine deficiency (PCD) is an autosomal recessive disorder of fatty acid oxidation, in which the transport of carnitine into cells is impaired. Carnitine plays an important role in transporting fatty acids into the mitochondria and carnitine de...

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Detalles Bibliográficos
Autores principales: Dehkordi, Elham Hashemi, Sobhani, Payam, Asadpour, Nabiolah, Hashemipour, Mahin, Mostofizadeh, Neda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050976/
https://www.ncbi.nlm.nih.gov/pubmed/30069437
http://dx.doi.org/10.4103/2277-9175.235779

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050976/
https://www.ncbi.nlm.nih.gov/pubmed/30069437
http://dx.doi.org/10.4103/2277-9175.235779

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