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Article

Whole-exome sequencing confirmation of a novel heterozygous mutation in RUNX1 in a pregnant woman with platelet disorder.

Platelets - 1 Jan 2015

Obata Miyuki, Tsutsumi Seiji, Makino Satoshi, Takahashi Kanako, Watanabe Norikazu, Yoshida Takayuki, Tamiya Gen, Kurachi Hirohisa

Abstract excerpt

We describe a successful pregnancy and delivery in a patient with platelet disorder. Prophylactic platelet transfusions ensured that there were no bleeding complications during and after cesarean section. Following delivery, we performed whole exome sequencing, using next generation sequencing, t...

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Source

Identifiers

PMID: 24853048
DOI: 10.3109/09537104.2014.912750

Genes

RUNX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24853048-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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