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Autoimmunity Volume 52, 2019 - Issue 7-8
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Original Articles

Blau syndrome with a rare mutation in exon 9 of NOD2 gene

Jelena VelickovicFaculty of Medicine, Institute of Forensic Medicine, University of Belgrade, Belgrade, Serbia; Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-4834-8044View further author information
ORCID Icon,
Fatma SilanFaculty of Medicine, Department of Medical Genetic, COMU University, Canakkale, Turkey; View further author information
,
Firdevs Dincsoy BirFaculty of Medicine, Department of Medical Genetic, COMU University, Canakkale, Turkey; View further author information
,
Coskun SilanFaculty of Medicine, Department of Pharmacology, COMU University, Canakkale, TurkeyView further author information
,
Burcu AlbuzFaculty of Medicine, Department of Medical Genetic, COMU University, Canakkale, Turkey; View further author information
&
Ozturk OzdemirFaculty of Medicine, Department of Medical Genetic, COMU University, Canakkale, Turkey; View further author information
Pages 256-263 | Received 14 Mar 2019, Accepted 19 Sep 2019, Published online: 26 Sep 2019

References

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