Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex

Tuberous sclerosis complex (TSC) is an autosomal dominant disease caused by loss-of-function mutations in either of two tumor suppressor genes, TSC1 and TSC2. These mutations lead to the growth of benign tumors and hamartomas in many organs, including those of the central nervous system, the skin, a...

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Detalles Bibliográficos
Autores principales: Muto, Yoshinari, Sasaki, Hitomi, Sumitomo, Makoto, Inagaki, Hidehito, Kato, Maki, Kato, Takema, Miyai, Shunsuke, Kurahashi, Hiroki, Shiroki, Ryoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831580/
https://www.ncbi.nlm.nih.gov/pubmed/35145067
http://dx.doi.org/10.1038/s41439-022-00181-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831580/
https://www.ncbi.nlm.nih.gov/pubmed/35145067
http://dx.doi.org/10.1038/s41439-022-00181-1

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