Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan
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DOI: 10.1371/journal.pone.0211261
Abstract: Objectives To explore the molecular epidemiology of rare deafness genes in Taiwanese sensorineural hearing impairment (SNHI) patients with cochlear implantation (CI) by performing massive parallel sequencing (MPS) and correlating genetic factors and CI outcomes. Methods… read more here.
Keywords: patients cochlear; deafness genes; hearing; non syndromic ... See more keywords
Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia.
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DOI: 10.18632/oncotarget.18803
Abstract: Microtia is a congenital malformation of the external ear caused by genetic and/or environmental factors. However, no causal genetic mutations have been identified in isolated microtia patients. In this study, we utilized targeted genomic capturing… read more here.
Keywords: microtia; target sequencing; microtia patients; deafness genes ... See more keywords