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pro vyhledávání: '"Houcine Ben Ameur"'
Autor:
Yu-Lung Lau, Najla Mekki, Lamia Gargouri, Imen Ben-Mustapha, Rachida Boukari, Abdelhamid Barakat, Mohamed Bejaoui, Zahra Aadam, Jouda Gamara, Koon Wing Chan, Nabil BelHadj-Hmida, Aziz Bousfiha, Beya Larguèche, Houcine Ben Ameur, Jing Yang, Fethi Mellouli, Amel Nedri, Nadia Kechout, Mohamed-Ridha Barbouche, Meriem Ben-Ali
Publikováno v:
Journal of Clinical Immunology. 40:96-104
Autosomal recessive agammaglobulinemia (ARA) is a primary immunodeficiency characterized by absent peripheral B cells, severe hypogammaglobulinemia, and absent BTK gene mutations. In ARA, mutations occur in genes encoding the pre-B cell receptor (pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a703aff9a631b2c6baec96b2478f26a
https://doi.org/10.1007/s10875-019-00706-4
https://doi.org/10.1007/s10875-019-00706-4
