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pro vyhledávání: '"Bella Shadur"'
Autor:
Paul Edgar Gray, Bella Shadur, Susan Russell, Richard Mitchell, Michael Buckley, Kerri Gallagher, Ian Andrews, Kevin Thia, Joseph A. Trapani, Edwin Philip Kirk, Ilia Voskoboinik
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Bi-allelic null mutations affecting UNC13D, STXBP2, or STX11 result in defects of lymphocyte cytotoxic degranulation and commonly cause familial hemophagocytic lymphohistiocytosis (FHL) in early life. Patients with partial loss of function are increa
Externí odkaz:
https://doaj.org/article/9b1fec07a2704ab881fd21c60040f714
Autor:
Ilia Voskoboinik, Susan Russell, Michael F. Buckley, Edwin P. Kirk, Paul Gray, Kevin Y. T. Thia, Bella Shadur, Joseph A. Trapani, Kerri Gallagher, Richard Mitchell, Ian Andrews
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 8 (2017)
Frontiers in Immunology, Vol 8 (2017)
Bi-allelic null mutations affecting UNC13D, STXBP2 or STX11 result in defects of lymphocyte cytotoxic degranulation, and commonly cause familial haemophagocytic lymphohistiocytosis (FHL) in early life. Patients with partial loss of function are incre