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A rare splicing mutation in the PROS1 gene of a Korean patient with type I hereditary protein S deficiency.

Authors
  • 1
  • 1 Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea. , (North Korea)
Type
Published Article
Journal
Annals of clinical and laboratory science
1550-8080
Publication Date
Volume
41
Issue
4
Pages
397–400
Identifiers
PMID: 22166512
Source
Medline

Abstract

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