Browse

Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss

DC Field Value Language
dc.contributor.authorOziębło, Dominika-
dc.contributor.authorLee, Sang‐Yeon-
dc.contributor.authorLeja, Marcin Ludwik-
dc.contributor.authorSarosiak, Anna-
dc.contributor.authorBałdyga, Natalia-
dc.contributor.authorSkarżyński, Henryk-
dc.contributor.authorKim, Yehree-
dc.contributor.authorHan, Jin Hee-
dc.contributor.authorYoo, Hyo Soon-
dc.contributor.authorPark, Min Hyun-
dc.contributor.authorChoi, Byung Yoon-
dc.contributor.authorOłdak, Monika-
dc.date.accessioned2022-06-23T03:58:09Z-
dc.date.available2022-06-23T03:58:09Z-
dc.date.created2022-05-10-
dc.date.issued2022-04-
dc.identifier.citationHuman Genetics, Vol.141 No.3-4, pp.445-453-
dc.identifier.issn0340-6717-
dc.identifier.urihttps://hdl.handle.net/10371/183690-
dc.description.abstract© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.Novel hearing loss (HL) genes are constantly being discovered, and evidence from independent studies is essential to strengthen their position as causes of hereditary HL. To address this issue, we searched our genetic data of families with autosomal dominant HL (ADHL) who had been tested with high-throughput DNA sequencing methods. For CD164, only one pathogenic variant in one family has so far been reported. For LMX1A, just two previous studies have revealed its involvement in ADHL. In this study we found two families with the same pathogenic variant in CD164 and one family with a novel variant in LMX1A (c.686C>A; p.(Ala229Asp)) that impairs its transcriptional activity. Our data show recurrence of the same CD164 variant in two HL families of different geographic origin, which strongly suggests it is a mutational hotspot. We also provide further evidence for haploinsufficiency as the pathogenic mechanism underlying LMX1A-related ADHL.-
dc.language영어-
dc.publisherSpringer Verlag-
dc.titleUpdate on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss-
dc.typeArticle-
dc.citation.journaltitleHuman Genetics-
dc.identifier.wosid000765690800001-
dc.identifier.scopusid2-s2.0-85125734959-
dc.citation.endpage453-
dc.citation.number3-4-
dc.citation.startpage445-
dc.citation.volume141-
dc.identifier.rimsid160695-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorLee, Sang‐Yeon-
dc.contributor.affiliatedAuthorPark, Min Hyun-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Dept. of Medicine (의학과)Journal Papers (저널논문_의학과)
Files in This Item:
There are no files associated with this item.
  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse