Affordable Access

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

Authors
Type
Published Article
Journal
Annals of clinical and laboratory science
Publication Date
Volume
41
Issue
4
Pages
397–400
Identifiers
PMID: 22166512
Source
Medline

Abstract

There are no comments yet on this publication. Be the first to share your thoughts.

Statistics

Seen <100 times
0 Comments