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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) ORCID logo https://orcid.org/0000-0002-0608-2989
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/150029
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