A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2.
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| Title: | A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2. |
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| Authors: | Chepurwar S; Institute for Auditory Neuroscience and SFB889, Göttingen University Medical Center, Göttingen 37075, Germany., von Loh SM; Institute for Human Genetics, University Hospital Hamburg-Eppendorf, Hamburg 20246, Germany., Wigger DC; Institute of Human Genetics, University of Ulm, Ulm 89081, Germany., Neef J; Institute for Auditory Neuroscience and SFB889, Göttingen University Medical Center, Göttingen 37075, Germany., Frommolt P; Institute for Human Genetics, University Hospital Hamburg-Eppendorf, Hamburg 20246, Germany., Beutner D; Department of Otorhinolaryngology, Head and Neck Surgery, Göttingen University Medical Center, Göttingen 37075, Germany.; Department of Otorhinolaryngology, Head and Neck Surgery, University of Cologne, Cologne 50931, Germany., Lang-Roth R; Department of Otorhinolaryngology, Head and Neck Surgery, University of Cologne, Cologne 50931, Germany., Kubisch C; Institute for Human Genetics, University Hospital Hamburg-Eppendorf, Hamburg 20246, Germany., Strenzke N; Institute for Auditory Neuroscience and SFB889, Göttingen University Medical Center, Göttingen 37075, Germany., Volk AE; Institute for Human Genetics, University Hospital Hamburg-Eppendorf, Hamburg 20246, Germany. |
| Source: | Human molecular genetics [Hum Mol Genet] 2023 Mar 20; Vol. 32 (7), pp. 1083-1089. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1460-2083 |
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| DOI: | 10.1093/hmg/ddac267 |
