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pro vyhledávání: '"Yavuz Köker"'
Autor:
M de Boer, Ahmet Metin, Ozden Sanal, Ilhan Tezcan, Dirk Roos, Tuba Turul Ozgur, K. van Leeuwen, Mustafa Yavuz Köker, Fatih Celmeli
Publikováno v:
European journal of clinical investigation, 39(4), 311-319. Wiley-Blackwell
Background One of the rarest forms of autosomal recessive chronic granulomatous disease (AR-CGD) is attributable to mutations in the CYBA gene, which encodes the alpha polypeptide of cytochrome b558, (also known as p22-phox), a key transmembrane prot