Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.
Publication year
1999Source
Journal of Neurology, Neurosurgery, and Psychiatry, 66, (1999), pp. 569-574ISSN
Publication type
Article / Letter to editor
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Organization
Neurology
Human Genetics
Pathology
Journal title
Journal of Neurology, Neurosurgery, and Psychiatry
Volume
vol. 66
Page start
p. 569
Page end
p. 574
Subject
Hereditary motor and sensory neuropathies.; Analysis of mitochondrial DNA as part of the diagnosis of mitochondrial myopathies; Hereditaire motore en sensore neuropathieën.; Onderzoek van mitochondrieel DNA in het kader van diagnostiek van mitochondriële myopathieenThis item appears in the following Collection(s)
- Academic publications [246764]
- Faculty of Medical Sciences [93461]
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