TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad.
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| Title: | TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad. |
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| Authors: | Guillen-Ahlers H; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA., Erbe CB; Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, WI, USA., Chevalier FD; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA., Montoya MJ; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA., Zimmerman KD; Department of Biostatistical Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA., Langefeld CD; Department of Biostatistical Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA., Olivier M; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA., Runge CL; Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, WI, USA. |
| Source: | Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2018 Jul; Vol. 6 (4), pp. 653-659. Date of Electronic Publication: 2018 Apr 19. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2324-9269 (Electronic) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: MEDLINE; PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2324-9269 |
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| DOI: | 10.1002/mgg3.397 |
