Molecular and clinical analyses of 84 patients with tuberous sclerosis complex

BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant disease characterized by the development of multiple hamartomas in many internal organs. Mutations in either one of 2 genes, TSC1 and TSC2, have been attributed to the development of TSC. More than two-thirds of TSC patients are s...

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Detalles Bibliográficos
Autores principales: Hung, Chia-Cheng, Su, Yi-Ning, Chien, Shu-Chin, Liou, Horng-Huei, Chen, Chih-Chuan, Chen, Pau-Chung, Hsieh, Chia-Jung, Chen, Chih-Ping, Lee, Wang-Tso, Lin, Win-Li, Lee, Chien-Nan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592085/
https://www.ncbi.nlm.nih.gov/pubmed/16981987
http://dx.doi.org/10.1186/1471-2350-7-72

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592085/
https://www.ncbi.nlm.nih.gov/pubmed/16981987
http://dx.doi.org/10.1186/1471-2350-7-72

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