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- W2059982011 abstract "Tuberous sclerosis complex (TSC), also known as Bourneville disease or tuberous sclerosis, is a multisystem disease characterized by the formation of hamartomatous growths, caused by inactivating mutations at 1 of 2 genetic loci.1 TSC 1 is located at chromosome 9q34, the product of which is known as hamartin. Tuberous sclerosis complex 2 (TSC2) is a gene located on chromosome 16p13 and is more commonly implicated in cases of sporadic TSC.1 The TSC2 product is known as tuberin, and TSC2 mutations may be associated with more severe disease." @default.
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- W2059982011 date "2012-11-01" @default.
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- W2059982011 title "Multiple Impacted Teeth and Associated Pericoronal Tissue Abnormality in Tuberous Sclerosis Complex" @default.
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- W2059982011 doi "https://doi.org/10.1016/j.joms.2011.12.003" @default.
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