Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse

By Rhead W.J.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2069-2077

Oxford University Press

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Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders

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Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2695-2703

Oxford University Press

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Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy

By Unterrainer Gertraud   Molzer Brunhilde   Forss-Petter Sonja   Berger Johannes  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2609-2616

Oxford University Press

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Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency

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Human Molecular Genetics, Vol. 14, Iss. 9, 2005-05 ,pp. : 1127-1137

Oxford University Press

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Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28

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Human Genetics, Vol. 114, Iss. 3, 2004-02 ,pp. : 298-305

Springer Publishing Company

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