Identification of a region required for TSC1 stability by functional analysis of <it>TSC1 </it>missense mutations found in individuals with tuberous sclerosis complex
<p>Abstract</p> <p>Background</p> <p>Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterised by the development of hamartomas in a variety of organs and tissues. The disease is caused by mutations in either the <it>TSC1 </it>gene on...
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| Main Authors: | , , , , , , , , , |
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| Format: | Book |
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BMC,
2009-09-01T00:00:00Z.
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