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.