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

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

Book ID: 125491234
Publisher: Informa plc
Year: 2014
Tongue: English
Weight: 420 KB
Volume: 26
Category: Article
ISSN: 0953-7104
DOI: 10.3109/09537104.2014.912750

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