Condition: Recurrent otitis media
rs1057524157
in
DEAF1
gene and
Recurrent otitis media
PMID 28213671
2017 Exome analysis of Smith-Magenis-like syndrome cohort identifies de novo likely pathogenic variants.
PMID 28940898
2017 Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype.
rs527656756
in
MTA3;HAAO
gene and
Recurrent otitis media
PMID 28792876
2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.