Ontology highlight
ABSTRACT:
SUBMITTER: Schilit SL
PROVIDER: S-EPMC5110062 | biostudies-literature | 2016 Nov
REPOSITORIES: biostudies-literature
Schilit Samantha Lp SL Currall Benjamin B BB Yao Ruen R Hanscom Carrie C Collins Ryan L RL Pillalamarri Vamsee V Lee Dong-Young DY Kammin Tammy T Zepeda-Mendoza Cinthya J CJ Mononen Tarja T Nolan Lisa S LS Gusella James F JF Talkowski Michael E ME Shen Jun J Morton Cynthia C CC
European journal of human genetics : EJHG 20160706 11
Analysis of chromosomal rearrangements has been highly successful in identifying genes involved in many congenital abnormalities including hearing loss. Herein, we report a subject, designated DGAP242, with congenital hearing loss (HL) and a de novo balanced translocation 46,XX,t(1;5)(q32;q15)dn. Using multiple next-generation sequencing techniques, we obtained high resolution of the breakpoints. This revealed disruption of the orphan receptor ESRRG on chromosome 1, which is differentially expre ...[more]