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Article

A neonate bearing a novel genetic variant within the factor XIII active site presenting with severe umbilical haemorrhage.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Nov 2020

Strumph Kaitlin, Davila Jennifer, Mitchell William B

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Share to Catalytic Domain
Share to Factor XIII
Share to Genetic Variation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to High-Throughput Nucleotide Sequencing

Share to Infant, Newborn

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Identifiers

PMID: 32558089
DOI: 10.1111/hae.14074

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A neonate bearing a novel genetic variant within the factor XIII active site presenting with severe umbilical haemorrhage.PMID 32558089Read ↗

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