Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Robin Vlamis"'
Autor:
Lara Rodríguez-Laguna, Kristen Davis, Mellenee Finger, Dawn Aubel, Robin Vlamis, Craig Johnson
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background PROS disorders are driven by somatic, gain-of-function mutations in PIK3CA that result in hyperactivation of the phosphatidylinositol-3-kinase (PI3K) signaling pathway. PROS encompasses a broad spectrum of overlapping phenotypes (
Externí odkaz:
https://doaj.org/article/340ef9c9e2884402a61ae9466d67dc8e
Autor:
Lara Rodríguez-Laguna, Kristen Davis, Mellenee Finger, Dawn Aubel, Robin Vlamis, Craig Johnson
Publikováno v:
Orphanet journal of rare diseases. 17(1)
Background PROS disorders are driven by somatic, gain-of-function mutations in PIK3CA that result in hyperactivation of the phosphatidylinositol-3-kinase (PI3K) signaling pathway. PROS encompasses a broad spectrum of overlapping phenotypes (including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f00b1323bf3d546d8b2c1782f19d262
https://pubmed.ncbi.nlm.nih.gov/35526022
https://pubmed.ncbi.nlm.nih.gov/35526022