Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

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Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

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2018 nî lūn-bûn

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Genetic variation in the C-typ ...... n Willebrand Disease patients.

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Genetic variation in the C-typ ...... n Willebrand Disease patients.

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Genetic variation in the C-typ ...... n Willebrand Disease patients.

@en

Genetic variation in the C-typ ...... n Willebrand Disease patients.

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Genetic variation in the C-typ ...... n Willebrand Disease patients.

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Genetic variation in the C-typ ...... n Willebrand Disease patients.

@nl

P1476

Genetic variation in the C-typ ...... n Willebrand Disease patients.

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Christer Halldén

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Christina Lind-Halldén

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Stefan Lethagen

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P2860

Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels

PLINK: a tool set for whole-genome association and population-based linkage analyses

Haploview: analysis and visualization of LD and haplotype maps

The origin and evolution of variable number tandem repeat of CLEC4M gene in the global human population

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

MutationTaster evaluates disease-causing potential of sequence alterations

Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

The heritage of pathogen pressures and ancient demography in the human innate-immunity CD209/CD209L region

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Effect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients.

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e0192024

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scholarly article

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10.1371/JOURNAL.PONE.0192024

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English

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P478

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Eric Manderstedt

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2018-02-01T00:00:00Z

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29389944

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5794141

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