Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Fahad Almodaihsh"'
Autor:
Musa Alzahrani, Saeed Al Turki, Waleed Al Rajban, Fatimah Alshalati, Fahad Almodaihsh, Khadega A. Abuelgasim, Bader Alahmari, Thamer Al Bogami, Osama Ali, Talal Al Harbi, Mohammed A. AlBalwi, Maram Alotaibi, Aamer Aleem, Ahmed Al Asker, Areej Al Mugairi
Publikováno v:
Platelets, Vol 33, Iss 8, Pp 1220-1227 (2022)
The P106L mutation in the human myeloproliferative leukemia virus oncogene (MPL) was shown to be associated with hereditary thrombocythemia in Arabs. The clinical and bone marrow (BM) features of P106L mutation are unknown. Genetic databases at two t
Externí odkaz:
https://doaj.org/article/b3dfdcf067bd4384bbe486c95c270452
Autor:
Aamer Aleem, Areej Al Mugairi, Saeed Al Turki, Musa Alzahrani, Fahad Almodaihsh, Ahmed Alaskar, Thamer Al Bogami, Osama Ali, Khadega A. Abuelgasim, Maram Alotaibi, Fatimah Alshalati, Bader Alahmari, Waleed Al Rajban
Publikováno v:
Blood. 136:7-8
Background: Hereditary thrombocythemia (HT) has been reported in Japanese and African populations in association with S505N, and N35K c-Mpl mutations, respectively. A novel Pro106Leu germ-line mutation in the c-Mpl gene has recently been shown to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7719f791e6bd788ac9fa1fd93cf6537a
https://doi.org/10.1182/blood-2020-136077
https://doi.org/10.1182/blood-2020-136077