View in EDS HTML Full Text PDF Full Text

Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss.

Saved in:
Bibliographic Details
Title: Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss.
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
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 34733312
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Booth+KT%22">Booth KT</searchLink>; Department of Neurobiology, Harvard Medical School, Boston, MA, United States.<br /><searchLink fieldCode="AU" term="%22Hirsch+Y%22">Hirsch Y</searchLink>; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Brooklyn, NY, United States.<br /><searchLink fieldCode="AU" term="%22Vardaro+AC%22">Vardaro AC</searchLink>; Department of Neurobiology, Harvard Medical School, Boston, MA, United States.<br /><searchLink fieldCode="AU" term="%22Ekstein+J%22">Ekstein J</searchLink>; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Brooklyn, NY, United States.<br /><searchLink fieldCode="AU" term="%22Yefet+D%22">Yefet D</searchLink>; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Quint+A%22">Quint A</searchLink>; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Weiden+T%22">Weiden T</searchLink>; Dor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.<br /><searchLink fieldCode="AU" term="%22Corey+DP%22">Corey DP</searchLink>; Department of Neurobiology, Harvard Medical School, Boston, MA, United States.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2021 Oct 18; Vol. 12, pp. 737782. <i>Date of Electronic Publication: </i>2021 Oct 18 (<i>Print Publication: </i>2021).
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560621 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-8021 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216648021%22">16648021 </searchLink><i>NLM ISO Abbreviation: </i>Front Genet <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=34733312
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.3389/fgene.2021.737782
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 737782
    Titles:
      – TitleFull: Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Booth KT
      – PersonEntity:
          Name:
            NameFull: Hirsch Y
      – PersonEntity:
          Name:
            NameFull: Vardaro AC
      – PersonEntity:
          Name:
            NameFull: Ekstein J
      – PersonEntity:
          Name:
            NameFull: Yefet D
      – PersonEntity:
          Name:
            NameFull: Quint A
      – PersonEntity:
          Name:
            NameFull: Weiden T
      – PersonEntity:
          Name:
            NameFull: Corey DP
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 18
              M: 10
              Text: 2021 Oct 18
              Type: published
              Y: 2021
          Identifiers:
            – Type: issn-print
              Value: 1664-8021
          Numbering:
            – Type: volume
              Value: 12
          Titles:
            – TitleFull: Frontiers in genetics
              Type: main
ResultId 1