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pro vyhledávání: '"Jelena Maletkovic-Barjaktarevic"'
Publikováno v:
Medical Hypotheses. 74:445-448
Reticular dysgenesis (RD) is a rare form of severe combined immunodeficiency (SCID). The underlying genetic defect for most cases of RD was recently identified in the gene encoding adenylate kinase 2 (AK2). However, rare patients with RD and no mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf3df3ab426dd47b6a1f9cf23d183ae
https://doi.org/10.1016/j.mehy.2009.09.053
https://doi.org/10.1016/j.mehy.2009.09.053
