Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype.
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| Title: | Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype. |
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| Authors: | EL Bouchikhi, Ihssane1,2 (AUTHOR) ihssane.elbouchikhi@usmba.ac.ma, Belhassan, Khadija1 (AUTHOR), Moufid, Fatima Zohra1 (AUTHOR), Bouguenouch, Laila1 (AUTHOR), Samri, Imane1 (AUTHOR), Iraqui Houssaïni, Mohammed3 (AUTHOR), Ouldim, Karim1 (AUTHOR), Atmani, Samir4 (AUTHOR) |
| Source: | Egyptian Journal of Medical Human Genetics. 3/11/2021, Vol. 22 Issue 1, p1-7. 7p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 149171961 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22EL+Bouchikhi%2C+Ihssane%22">EL Bouchikhi, Ihssane</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> ihssane.elbouchikhi@usmba.ac.ma</i><br /><searchLink fieldCode="AR" term="%22Belhassan%2C+Khadija%22">Belhassan, Khadija</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Moufid%2C+Fatima+Zohra%22">Moufid, Fatima Zohra</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bouguenouch%2C+Laila%22">Bouguenouch, Laila</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Samri%2C+Imane%22">Samri, Imane</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Iraqui+Houssaïni%2C+Mohammed%22">Iraqui Houssaïni, Mohammed</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ouldim%2C+Karim%22">Ouldim, Karim</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Atmani%2C+Samir%22">Atmani, Samir</searchLink><relatesTo>4</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Egyptian+Journal+of+Medical+Human+Genetics%22">Egyptian Journal of Medical Human Genetics</searchLink>. 3/11/2021, Vol. 22 Issue 1, p1-7. 7p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=149171961 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s43042-021-00136-1 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 1 Titles: – TitleFull: Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: EL Bouchikhi, Ihssane – PersonEntity: Name: NameFull: Belhassan, Khadija – PersonEntity: Name: NameFull: Moufid, Fatima Zohra – PersonEntity: Name: NameFull: Bouguenouch, Laila – PersonEntity: Name: NameFull: Samri, Imane – PersonEntity: Name: NameFull: Iraqui Houssaïni, Mohammed – PersonEntity: Name: NameFull: Ouldim, Karim – PersonEntity: Name: NameFull: Atmani, Samir IsPartOfRelationships: – BibEntity: Dates: – D: 11 M: 03 Text: 3/11/2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 11108630 Numbering: – Type: volume Value: 22 – Type: issue Value: 1 Titles: – TitleFull: Egyptian Journal of Medical Human Genetics Type: main |
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