Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece

Tuberous sclerosis complex (TSC) is a rare autosomal dominant disorder causing benign tumors in the brain and other vital organs. The genes implicated in disease development are TSC1 and TSC2. Here, we have performed mutational analysis followed by a genotype-phenotype correlation study based on the...

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Detalles Bibliográficos
Autores principales: Avgeris, Socratis, Fostira, Florentia, Vagena, Andromachi, Ninios, Yiannis, Delimitsou, Angeliki, Vodicka, Radek, Vrtel, Radek, Youroukos, Sotirios, Stravopodis, Dimitrios J., Vlassi, Metaxia, Astrinidis, Aristotelis, Yannoukakos, Drakoulis, Voutsinas, Gerassimos E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711901/
https://www.ncbi.nlm.nih.gov/pubmed/29196670
http://dx.doi.org/10.1038/s41598-017-16988-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711901/
https://www.ncbi.nlm.nih.gov/pubmed/29196670
http://dx.doi.org/10.1038/s41598-017-16988-w

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