Decoding of novel missense TSC2 gene variants using in-silico methods
Abstract Background Mutations in TSC1 or TSC2 gene cause tuberous sclerosis complex (TSC), an autosomal dominant disorder characterized by the formation of non-malignant hamartomas in multiple vital organs. TSC1 and TSC2 gene products form TSC heterodimer that senses specific cell growth conditions...
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| Main Authors: | , , , , , , , , , |
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| Format: | Book |
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BMC,
2019-10-01T00:00:00Z.
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