Evidence for population variation in TSC1 and TSC2 gene expression
Evidence for population variation in TSC1 and TSC2 gene expression
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
Tuberous sclerosis complex (TSC) is an autosomal dominant neurogenetic disorder caused by mutations in one of two genes, TSC1 or TSC2, which encode the proteins hamartin and tuberin, respectively 123. Common features of TSC include intractable epilepsy, mental retardation, and autistic features. TSC is associated with specific brain lesions, includ...
Alternative Titles
Full title
Evidence for population variation in TSC1 and TSC2 gene expression
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TN_cdi_doaj_primary_oai_doaj_org_article_795019b545614d15870609778a29ffc6
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_795019b545614d15870609778a29ffc6
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ISSN
1471-2350
E-ISSN
1471-2350
DOI
10.1186/1471-2350-12-29
