Distinct clinical characteristics of Tuberous Sclerosis Complex patients with no mutation identified
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.2008.00496.x/fullpdf
Reference26 articles.
1. Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex;Ali;Acta Neurol Scand,2005
2. Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States;Au;Genet Med,2007
3. Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis;Carsillo;Proc Natl Acad Sci U S A,2000
4. The tuberous sclerosis complex;Crino;N Engl J Med,2006
5. Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs;Dabora;Am J Hum Genet,2001
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