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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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| Publicado no: | Adv Biomed Res |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6050976/ https://ncbi.nlm.nih.gov/pubmed/30069437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.235779 |
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