YUHSpace: Homozygous type I Protein C deficiency in neonatal purpura fulminans with a novel frame-shift deletion of 10 base pairs in exon 8 of PROC gene

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Homozygous type I Protein C deficiency in neonatal purpura fulminans with a novel frame-shift deletion of 10 base pairs in exon 8 of PROC gene

Authors: H. J. PARK ; K. S. SONG ; B. M. NAH ; J. R. CHOI ; M. J. KIM

Citation: JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol.3(3) : 593-595, 2005

Journal Title: JOURNAL OF THROMBOSIS AND HAEMOSTASIS

ISSN: 1538-7933

Issue Date: 2005

MeSH: DNA Mutational Analysis ; Exons ; Female ; Frameshift Mutation* ; Homozygote ; Humans ; Infant, Newborn ; Pregnancy ; Protein C/genetics* ; Protein C Deficiency/genetics* ; Purpura, Schoenlein-Henoch/genetics* ; Sequence Deletion

Keywords: 15748260

Full Text: http://onlinelibrary.wiley.com/doi/10.1111/j.1538-7836.2005.01144.x/abstract

DOI: 10.1111/j.1538-7836.2005.01144.x

Appears in Collections:: 1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

Yonsei Authors: Song, Kyung Soon(송경순)
Choi, Jong Rak(최종락) https://orcid.org/0000-0002-0608-2989

URI: https://ir.ymlib.yonsei.ac.kr/handle/22282913/150029

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