Identification of a Cowden syndrome patient with a novel PTEN mutation and establishment of patient-derived induced pluripotent stem cells

Cowden syndrome (CS) is an autosomal dominant inherited disorder characterized by multiple hamartomas in various organs such as the mucosa, skin, and gastrointestinal tract. Patients with CS are at high risk for breast and thyroid cancers. Phosphatase and tensin homolog deleted on chromosome 10 (PTE...

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Detalles Bibliográficos
Autores principales: Obayashi, Fumitaka, Hamada, Atsuko, Yamasaki, Sachiko, Kanda, Taku, Toratani, Shigeaki, Okamoto, Tetsuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803725/
https://www.ncbi.nlm.nih.gov/pubmed/34984555
http://dx.doi.org/10.1007/s11626-021-00637-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803725/
https://www.ncbi.nlm.nih.gov/pubmed/34984555
http://dx.doi.org/10.1007/s11626-021-00637-8

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