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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Adv Biomed Res |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Medknow Publications & Media Pvt Ltd
2018
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| Θέματα: | |
| Διαθέσιμο Online: | 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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