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

Subjects

Subjects :

Catalytic Domain
Female
Genetic Variation
High-Throughput Nucleotide Sequencing methods
Humans
Infant, Newborn
Male
Factor XIII genetics
Hemorrhage genetics
Umbilical Cord blood supply
Umbilicus pathology

Details

Language :

English

ISSN :

1365-2516

Volume :

26

Issue :

6

Database :

MEDLINE

Journal :

Haemophilia : the official journal of the World Federation of Hemophilia

Publication Type :

Report

Accession number :

32558089

Full Text :

https://doi.org/10.1111/hae.14074