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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.
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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  Data: TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad.
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  Data: <searchLink fieldCode="AU" term="%22Guillen-Ahlers+H%22">Guillen-Ahlers H</searchLink>; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.<br /><searchLink fieldCode="AU" term="%22Erbe+CB%22">Erbe CB</searchLink>; Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, WI, USA.<br /><searchLink fieldCode="AU" term="%22Chevalier+FD%22">Chevalier FD</searchLink>; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.<br /><searchLink fieldCode="AU" term="%22Montoya+MJ%22">Montoya MJ</searchLink>; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.<br /><searchLink fieldCode="AU" term="%22Zimmerman+KD%22">Zimmerman KD</searchLink>; Department of Biostatistical Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA.<br /><searchLink fieldCode="AU" term="%22Langefeld+CD%22">Langefeld CD</searchLink>; Department of Biostatistical Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA.<br /><searchLink fieldCode="AU" term="%22Olivier+M%22">Olivier M</searchLink>; Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, USA.<br /><searchLink fieldCode="AU" term="%22Runge+CL%22">Runge CL</searchLink>; Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, WI, USA.
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  Data: <searchLink fieldCode="JN" term="%22101603758%22">Molecular genetics & genomic medicine</searchLink> [Mol Genet Genomic Med] 2018 Jul; Vol. 6 (4), pp. 653-659. <i>Date of Electronic Publication: </i>2018 Apr 19.
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        Value: 10.1002/mgg3.397
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              Text: 2018 Jul
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