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Autor:
Delia Nicoară, Cristina Niță, Ana Stanilă, Alexandru Martiniuc, Laura Popa, Eliana Petrescu, Mihaela Bătăneant, Ruxandra Ciofu, Adriana Guriță, Radu Tabăcaru, Ruxandra Ionescu, Laura Groșeanu
Publikováno v:
Immunity, Inflammation and Disease, Vol 11, Iss 8, Pp n/a-n/a (2023)
Abstract Background The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease resulting from loss‐of‐function mutations in ADA2, formerly named CECR1 (cat eye syndrome chromosome region, candidate 1) gene. Dise
Externí odkaz:
https://doaj.org/article/c80790c648804cab8f681327b39215cb
