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Neonatal Carnitine Palmitoyltransferase II Deficiency: A Lethal Entity
Carnitine palmitoyltransferase II (CPTII) deficiency is a rare disorder of mitochondrial fatty acid oxidation with autosomal recessive mode of inheritance. Three classic forms of CPT II deficiency have been described namely the lethal neonatal form, severe infantile hepatocardiomuscular form and the...
Gardado en:
| Publicado en: | J Clin Diagn Res |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
JCDR Research and Publications (P) Limited
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4625305/ https://ncbi.nlm.nih.gov/pubmed/26557586 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2015/13600.6560 |
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