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