Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale

Autor:	Öztürk Özdemir, Coskun Silan, Jelena Djurovic, Fatma Silan, Firdevs Dincsoy Bir
Rok vydání:	2018
Předmět:	Genetics business.industry Bioengineering General Medicine medicine.disease Applied Microbiology and Biotechnology Exon Mutation (genetic algorithm) medicine Nod2 gene business Blau syndrome Biotechnology Rare disease
Zdroj:	Journal of Biotechnology. 280:S65
ISSN:	0168-1656
DOI:	10.1016/j.jbiotec.2018.06.213
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::0d90f6b1ec3f7e9a9d049737ee812049 https://doi.org/10.1016/j.jbiotec.2018.06.213 Zobrazit plný text záznamu Full Text from ScienceDirect