De novo CXCR4 Mutation in WHIM Syndrome: Report of a 4-Year-Old Case without Wart and Myelokathexis.
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| Title: | De novo CXCR4 Mutation in WHIM Syndrome: Report of a 4-Year-Old Case without Wart and Myelokathexis. |
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| Authors: | Roshdi, Shayan1,2, Shahkarami, Sepideh3,4, Zoghi, Samaneh4,5, Rayzan, Elham4, Molatefi, Rasol6, Rohlfs, Meino3, Klein, Christoph3, Rezaei, Nima4,7 rezaei_nima@tums.ac.ir |
| Source: | Immunology & Genetics Journal. 2025, Vol. 8 Issue 3, p303-307. 5p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 185376543 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=185376543 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.18502/igj.v8i3.18212 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 303 Titles: – TitleFull: De novo CXCR4 Mutation in WHIM Syndrome: Report of a 4-Year-Old Case without Wart and Myelokathexis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Roshdi, Shayan – PersonEntity: Name: NameFull: Shahkarami, Sepideh – PersonEntity: Name: NameFull: Zoghi, Samaneh – PersonEntity: Name: NameFull: Rayzan, Elham – PersonEntity: Name: NameFull: Molatefi, Rasol – PersonEntity: Name: NameFull: Rohlfs, Meino – PersonEntity: Name: NameFull: Klein, Christoph – PersonEntity: Name: NameFull: Rezaei, Nima IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: 2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 26454831 Numbering: – Type: volume Value: 8 – Type: issue Value: 3 Titles: – TitleFull: Immunology & Genetics Journal Type: main |
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