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carnitine deficient myopathy
Summary
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OMIM - Congenital disorder
OMIM - Metabolic disease
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Muscle carnitine deficiency: adult onset lipid storage myopathy with sensory neuropathy.
Genotype-phenotype correlation in primary carnitine deficiency.
Systemic primary carnitine deficiency: an overview of clinical manifestations, diagnosis, and manage…
SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case con…
Lipid storage myopathy with clinical markers of Marfan syndrome: A rare association.
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Identification of Carnitine-Responsive Cardiomyopathy
The Association of Genetic Polymorphisms With Statin-Induced Myopathy.
Effects of Parenteral L-carnitine Supplementation in Premature Neonates
Nephroprotective Effects of Carnitine and (PDE5) Inhibitor Agent Against Contrast Media-induced Neph…
Bezafibrate Trial in CPT2 Deficiency
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