Targeted next-generation sequencing for detection of PIK3CA mutations in archival tissues from patients with Klippel–Trenaunay syndrome in an Asian population: List the full names and institutional addresses for all authors

BACKGROUND: Klippel–Trenaunay syndrome (KTS) is a rare slow-flow combined vascular malformation with limb hypertrophy. KTS is thought to lie on the PIK3CA-related overgrowth spectrum, but reports are limited. PIK3CA encodes p110α, a catalytic subunit of phosphatidylinositol 3-kinase (PI3K) that play...

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Detalles Bibliográficos
Autores principales: Sasaki, Yuki, Ishikawa, Kosuke, Hatanaka, Kanako C., Oyamada, Yumiko, Sakuhara, Yusuke, Shimizu, Tadashi, Saito, Tatsuro, Murao, Naoki, Onodera, Tomohiro, Miura, Takahiro, Maeda, Taku, Funayama, Emi, Hatanaka, Yutaka, Yamamoto, Yuhei, Sasaki, Satoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478188/
https://www.ncbi.nlm.nih.gov/pubmed/37667289
http://dx.doi.org/10.1186/s13023-023-02893-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478188/
https://www.ncbi.nlm.nih.gov/pubmed/37667289
http://dx.doi.org/10.1186/s13023-023-02893-1

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