Haplotype-based association study of TCF7L2 gene variants with the development of diabetic retinopathy in an Iranian population.

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Title: Haplotype-based association study of TCF7L2 gene variants with the development of diabetic retinopathy in an Iranian population.
Authors: Alidoust, Leila1 (AUTHOR), Sharafshah, Alireza2,3 (AUTHOR), Keshavarz, Parvaneh2 (AUTHOR) keshavarz@gums.ac.ir
Source: Ophthalmic Genetics. Jun2024, Vol. 45 Issue 3, p226-232. 7p.
Database: Academic Search Ultimate
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An: 178881042
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  Data: Haplotype-based association study of TCF7L2 gene variants with the development of diabetic retinopathy in an Iranian population.
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  Data: <searchLink fieldCode="AR" term="%22Alidoust%2C+Leila%22">Alidoust, Leila</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sharafshah%2C+Alireza%22">Sharafshah, Alireza</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Keshavarz%2C+Parvaneh%22">Keshavarz, Parvaneh</searchLink><relatesTo>2</relatesTo> (AUTHOR)<i> keshavarz@gums.ac.ir</i>
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  Data: <searchLink fieldCode="JN" term="%22Ophthalmic+Genetics%22">Ophthalmic Genetics</searchLink>. Jun2024, Vol. 45 Issue 3, p226-232. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=178881042
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1080/13816810.2024.2318611
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 7
        StartPage: 226
    Titles:
      – TitleFull: Haplotype-based association study of TCF7L2 gene variants with the development of diabetic retinopathy in an Iranian population.
        Type: main
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      – PersonEntity:
          Name:
            NameFull: Alidoust, Leila
      – PersonEntity:
          Name:
            NameFull: Sharafshah, Alireza
      – PersonEntity:
          Name:
            NameFull: Keshavarz, Parvaneh
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          Dates:
            – D: 01
              M: 06
              Text: Jun2024
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-print
              Value: 13816810
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              Value: 45
            – Type: issue
              Value: 3
          Titles:
            – TitleFull: Ophthalmic Genetics
              Type: main
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