Muscle Carnitine Palmitoyltransferase II Deficiency: A Review of Enzymatic Controversy and Clinical Features

CPT (carnitine palmitoyltransferase) II muscle deficiency is the most common form of muscle fatty acid metabolism disorders. In contrast to carnitine deficiency, it is clinically characterized by attacks of myalgia and rhabdomyolysis without persistent muscle weakness and lipid accumulation in muscl...

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Detalles Bibliográficos
Autores principales: Lehmann, Diana, Motlagh, Leila, Robaa, Dina, Zierz, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297716/
https://www.ncbi.nlm.nih.gov/pubmed/28054946
http://dx.doi.org/10.3390/ijms18010082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297716/
https://www.ncbi.nlm.nih.gov/pubmed/28054946
http://dx.doi.org/10.3390/ijms18010082

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