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Article

Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia

3 Aug 2017

Abstract excerpt

allele variation in patients with SCA is clinically relevant, and NGS technology can offer a comprehensive alternative to targeted SNP-based testing. This is particularly relevant as NGS data becomes more widely available and could provide the means for reducing Rh alloimmunization in children with SCA.

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Share to Blood groups and transfusion
Share to Erythrocyte Function and Pathophysiology
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 29296782
DOI: 10.1182/bloodadvances.2017007898

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