Jelena Velickovic, Fatma Silan, Firdevs Dincsoy Bir, Coskun Silan, Burcu Albuz, & Ozturk Ozdemir. (2019). Blau syndrome with a rare mutation in exon 9 of NOD2 gene. Taylor & Francis Group.
Chicago Style (17th ed.) CitationJelena Velickovic, Fatma Silan, Firdevs Dincsoy Bir, Coskun Silan, Burcu Albuz, and Ozturk Ozdemir. Blau Syndrome with a Rare Mutation in Exon 9 of NOD2 Gene. Taylor & Francis Group, 2019.
MLA (9th ed.) CitationJelena Velickovic, et al. Blau Syndrome with a Rare Mutation in Exon 9 of NOD2 Gene. Taylor & Francis Group, 2019.
Warning: These citations may not always be 100% accurate.