Associated Papers
c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.
Dantas VG et al.
Genetics and Molecular Biology, 2014
No association of PTGDR -441C/T polymorphism with asthma in a North Indian population.
Birbian N et al.
Disease Markers, 2011
PTGDR is not a major candidate gene for asthma and atopy in Chinese children.
Leung TF et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology, 2009
Association of PTGDR gene polymorphisms with asthma in two Caucasian populations.
Zhu G et al.
Genes and Immunity, 2007
The PTGDR gene is not associated with asthma in 3 ethnically diverse populations.
Tsai YJ et al.
The Journal of Allergy and Clinical Immunology, 2006
Select a paper to view details