A Case Series of Adenosine Deaminase 2-deficient Patients Emphasizing Treatment and Genotype-phenotype Correlations
J Rheumatol
.
2015 Aug;42(8):1532-4.
doi: 10.3899/jrheum.150024.
Authors
Ezgi Deniz Batu
1
,
Omer Karadag
2
,
Ekim Zihni Taskiran
3
,
Umut Kalyoncu
2
,
Ivona Aksentijevich
4
,
Mehmet Alikasifoglu
5
,
Seza Özen
6
Affiliations
1
Department of Pediatrics, Division of Rheumatology;
2
Associate Professor, Department of Internal Medicine, Division of Rheumatology, Hacettepe University Faculty of Medicine;
3
Assistant Professor, Department of Medical Biology, Division of Rheumatology, Hacettepe University Faculty of Medicine;
4
Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA;
5
Professor, Department of Medical Genetics;
6
Professor, Department of Pediatrics, Division of Rheumatology, Hacettepe University Faculty of Medicine. sezaozen@hacettepe.edu.tr.
PMID:
26233953
DOI:
10.3899/jrheum.150024
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adenosine Deaminase / deficiency*
Child
Child, Preschool
Female
Genetic Association Studies
Genotype
Humans
Male
Phenotype
Substances
Adenosine Deaminase