Rhnull phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene.

Saved in:
Bibliographic Details
Title: Rhnull phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene.
Authors: Banerjee, Soumee1 (AUTHOR) soumee@bmstindia.org, Mathur, Ankit1 (AUTHOR), Hurkat, Neha2 (AUTHOR), Chakraborty, Santanu1 (AUTHOR), Reddy, T. V.1 (AUTHOR)
Source: Transfusion Medicine. Jun2024, Vol. 34 Issue 3, p223-226. 4p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 178178304
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Rh<subscript>null</subscript> phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Banerjee%2C+Soumee%22">Banerjee, Soumee</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> soumee@bmstindia.org</i><br /><searchLink fieldCode="AR" term="%22Mathur%2C+Ankit%22">Mathur, Ankit</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hurkat%2C+Neha%22">Hurkat, Neha</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chakraborty%2C+Santanu%22">Chakraborty, Santanu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Reddy%2C+T%2E+V%2E%22">Reddy, T. V.</searchLink><relatesTo>1</relatesTo> (AUTHOR)
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Transfusion+Medicine%22">Transfusion Medicine</searchLink>. Jun2024, Vol. 34 Issue 3, p223-226. 4p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=178178304
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1111/tme.13045
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 4
        StartPage: 223
    Titles:
      – TitleFull: Rhnull phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Banerjee, Soumee
      – PersonEntity:
          Name:
            NameFull: Mathur, Ankit
      – PersonEntity:
          Name:
            NameFull: Hurkat, Neha
      – PersonEntity:
          Name:
            NameFull: Chakraborty, Santanu
      – PersonEntity:
          Name:
            NameFull: Reddy, T. V.
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 06
              Text: Jun2024
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-print
              Value: 09587578
          Numbering:
            – Type: volume
              Value: 34
            – Type: issue
              Value: 3
          Titles:
            – TitleFull: Transfusion Medicine
              Type: main
ResultId 1