Author:
Bakker H. D.,Scholte H. R.,Jeneson J. A. L.,Busch H. F. M.,Abeling N. G. G. M.,van Gennip A. H.
Subject
Genetics (clinical),Genetics
Reference23 articles.
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2. Arts WFM, Scholte HR, Lonnen MCB et al (1987) Cytochromec oxidase deficiency in subacute necrotizing encephalomyelopathy.J Neurol Sci 77: 103?115.
3. Bakker HD, Scholte HR, Van den Bogert C et al (1993a) Deficiency of the adenine nucleotide translocator in muscle of a patient with myopathy and lactic acidosis: a new mitochondrial defect.Pediatr Res 33: 412?417.
4. Bakker HD, Scholte HR, Jeneson JAL (1993b) Vitamin E in a mitochondrial myopathy with proliferating mitochondria.Lancet 342: 175?176.
5. Barth PG, Scholte HR, Berden JA et al (1983) An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.J Neurol Sci 62: 327?355.
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