The effect of valinomycin in fibroblasts from patients with fatty acid oxidation disorders

Author:

Ndukwe Erlingsson Uzochi Chimdinma,Iacobazzi Francesco,Liu Aiping,Ardon Orly,Pasquali Marzia,Longo Nicola

Funder

National Institutes of Health

NIH

Dottorato in Morfobiologia Applicata e Citometabolismo dei Farmaci

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference17 articles.

1. Disorders of carnitine transport and the carnitine cycle;Longo;Am. J. Med. Genet.,2006

2. Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening;Spiekerkoetter;J. Inherit. Metab. Dis.,2010

3. N.D. Leslie, B.T. Tinkle, A.W. Strauss, K. Shooner, K. Zhang, Very long-chain acyl-coenzyme a dehydrogenase deficiency, in: R.A. Pagon, T.D. Bird, C.R. Dolan, K. Stephens, M.P. Adam (Eds.), GeneReviews™, Seattle (WA), University of Washington, Seattle, 1993-2013.

4. A general introduction to the biochemistry of mitochondrial fatty acid beta-oxidation;Houten;J. Inherit. Metab. Dis.,2010

5. Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels;Liebig;Pediatrics,2006

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