Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuber...
Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex
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England: BioMed Central Ltd
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English
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England: BioMed Central Ltd
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Tuberous sclerosis complex (TSC) is an autosomal dominant disorder that is associated with neurological symptoms, including autism spectrum disorder. Tuberous sclerosis complex is caused by pathogenic germline mutations of either the TSC1 or TSC2 gene, but somatic mutations were identified in both genes, and the combined effects of TSC1 and TSC2 mu...
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Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex
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TN_cdi_doaj_primary_oai_doaj_org_article_a39b296936a646239a528d815f67eade
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a39b296936a646239a528d815f67eade
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ISSN
1479-7364,1473-9542
E-ISSN
1479-7364
DOI
10.1186/s40246-023-00450-2
