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Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease).

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第一作者： Zhihui,Xie

第一单位： Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA.

作者： Zhihui,Xie ^[1] ; Vijayaraj,Nagarajan ^[2] ; Daniel E,Sturdevant ^[3] ; Shoko,Iwaki ^[1] ; Eunice,Chan ^[1] ; Laura,Wisch ^[1] ; Michael,Young ^[4] ; Celeste M,Nelson ^[1] ; Stephen F,Porcella ^[3] ; Kirk M,Druey ^[1]

作者单位： Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA. ^[1] Computational Biology Section; Bioinformatics and Computational Biosciences Branch; OCICB; NIAID/NIH; Bethesda, MD USA. ^[2] Genomics Unit, Research Technologies Section; Rocky Mountain Laboratories; NIAID/NIH, Hamilton, MT USA. ^[3] Clinical Research Directorate/CMRP; SAIC-Frederick, Inc; Frederick National Laboratory for Clinical Research; Frederick, MD USA. ^[4]

关键词 cell adhesion cell junction cytoskeleton genetics, genome-wide SNP study systemic capillary leak syndrome vascular permeability

DOI 10.4161/rdis.27445

PMID 24808988

发布时间 2025-05-29

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Rare diseases (Austin, Tex.)

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Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease).

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Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease).

Rare diseases (Austin, Tex.)

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Rare diseases (Austin, Tex.)

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