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pubmed-article:12891682pubmed:abstractTextWe report an autopsied case of a 21-gestational-week fetus with duplication of the proteolipid protein (PLP) gene (PLP1). An immunohistochemical study, which can detect the specific expression of PLP, myelin basic protein, myelin-associated glycoprotein, and platelet-derived growth factor receptor alpha subunit in brain tissues, showed that the myelination was almost the same as that of age-matched controls. This result suggests that the development and migration of the oligodendrocyte is normal in Pelizaeus-Merzbacher disease until midgestation. To our knowledge, this is the first report of the myelination of a fetus with duplication of the PLP1 gene.lld:pubmed
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pubmed-article:12891682pubmed:authorpubmed-author:KubotaTakeoTlld:pubmed
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pubmed-article:12891682pubmed:pagination259-62lld:pubmed
pubmed-article:12891682pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:12891682pubmed:year2003lld:pubmed
pubmed-article:12891682pubmed:articleTitleMyelination of a fetus with Pelizaeus-Merzbacher disease: immunopathological study.lld:pubmed
pubmed-article:12891682pubmed:affiliationDepartment of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.lld:pubmed
pubmed-article:12891682pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12891682pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed