A Novel Missense Variant in LMX1A Leads to Autosomal Dominant Nonsyndromic Hearing Loss.

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Bibliographic Details
Title: A Novel Missense Variant in LMX1A Leads to Autosomal Dominant Nonsyndromic Hearing Loss.
Authors: Chen R; Miller School of Medicine, University of Miami, Miami, Florida, USA., Swols DM; Miller School of Medicine, University of Miami, Miami, Florida, USA.; Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, USA., Bademci G; Miller School of Medicine, University of Miami, Miami, Florida, USA.; Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, USA., Tekin M; Miller School of Medicine, University of Miami, Miami, Florida, USA.; Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, USA.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2026 Feb; Vol. 200 (2), pp. 531-534. Date of Electronic Publication: 2025 Oct 13.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1552-4833
DOI:10.1002/ajmg.a.64281