Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss.
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| Title: | Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss. |
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| Authors: | Booth KT; Department of Neurobiology, Harvard Medical School, Boston, MA, United States., Hirsch Y; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Brooklyn, NY, United States., Vardaro AC; Department of Neurobiology, Harvard Medical School, Boston, MA, United States., Ekstein J; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Brooklyn, NY, United States., Yefet D; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel., Quint A; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel., Weiden T; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel., Corey DP; Department of Neurobiology, Harvard Medical School, Boston, MA, United States. |
| Source: | Frontiers in genetics [Front Genet] 2021 Oct 18; Vol. 12, pp. 737782. Date of Electronic Publication: 2021 Oct 18 (Print Publication: 2021). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1664-8021 |
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| DOI: | 10.3389/fgene.2021.737782 |
