Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Malé Doré"'
Publikováno v:
The Pan African Medical Journal, Vol 36, Iss 385 (2020)
X-linked agammaglobulinemia (XLA) is a rare genetic disease caused by a mutation in the Bruton tyrosine kinase (BTK) gene. It is characterized by a profound deficiency of B cells and a decrease in all classes of immunoglobulins (Ig). We report one ca
Externí odkaz:
https://doaj.org/article/f8fdba032c9a45d7adde24c22666827b
Autor:
Mohamed Lamine Condé, Souleymane Djigué Barry, Mohamed Lamine Touré, Mohamed Tafsir Diallo, Mouloukou Souleymane Doumbouya, Malé Doré, Idrissa Aissatou Camara, Laila Touré, Karinka Diawara, Namory Camara, Idrissa Doumbouya, Gnouma Sidibé, Mohamed Asmaouh Bangoura, Fodé Abass Cissé
Publikováno v:
OALib. :1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abdacd716bec64bfce38740bd96cd82e
https://doi.org/10.4236/oalib.1109332
https://doi.org/10.4236/oalib.1109332
Publikováno v:
The Pan African Medical Journal
Pan African Medical Journal; Vol. 36 No. 1 (2020)
Pan African Medical Journal; Vol. 36 No. 1 (2020)
X-linked agammaglobulinemia (XLA) is a rare genetic disease caused by a mutation in the Bruton tyrosine kinase (BTK) gene. It is characterized by a profound deficiency of B cells and a decrease in all classes of immunoglobulins (Ig). We report one ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::348b49847c574c315962098a959b2aeb
http://europepmc.org/articles/PMC7666687
http://europepmc.org/articles/PMC7666687