Novel variant in WT1 gene associated with MGD and unique kidney disease phenotype.
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| Title: | Novel variant in WT1 gene associated with MGD and unique kidney disease phenotype. |
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| Authors: | Hassan, Heba A.1,2 (AUTHOR) heba.amin@yahoo.com, Mazen, Inas2,3 (AUTHOR), Mekkawy, Mona K.2,4 (AUTHOR), Elaidy, Aya2,3 (AUTHOR), Kamel, Alaa2,4 (AUTHOR), Essawi, Mona L.1,2 (AUTHOR) |
| Source: | Journal of Rare Diseases. 3/3/2025, Vol. 4 Issue 1, p1-7. 7p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 183406649 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Novel variant in WT1 gene associated with MGD and unique kidney disease phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Hassan%2C+Heba+A%2E%22">Hassan, Heba A.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> heba.amin@yahoo.com</i><br /><searchLink fieldCode="AR" term="%22Mazen%2C+Inas%22">Mazen, Inas</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mekkawy%2C+Mona+K%2E%22">Mekkawy, Mona K.</searchLink><relatesTo>2,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Elaidy%2C+Aya%22">Elaidy, Aya</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kamel%2C+Alaa%22">Kamel, Alaa</searchLink><relatesTo>2,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Essawi%2C+Mona+L%2E%22">Essawi, Mona L.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Rare+Diseases%22">Journal of Rare Diseases</searchLink>. 3/3/2025, Vol. 4 Issue 1, p1-7. 7p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=183406649 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s44162-025-00070-5 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 1 Titles: – TitleFull: Novel variant in WT1 gene associated with MGD and unique kidney disease phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Hassan, Heba A. – PersonEntity: Name: NameFull: Mazen, Inas – PersonEntity: Name: NameFull: Mekkawy, Mona K. – PersonEntity: Name: NameFull: Elaidy, Aya – PersonEntity: Name: NameFull: Kamel, Alaa – PersonEntity: Name: NameFull: Essawi, Mona L. IsPartOfRelationships: – BibEntity: Dates: – D: 03 M: 03 Text: 3/3/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 2731085X Numbering: – Type: volume Value: 4 – Type: issue Value: 1 Titles: – TitleFull: Journal of Rare Diseases Type: main |
| ResultId | 1 |