Recurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X Deficiency
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Date
2011
Journal Title
Journal ISSN
Volume Title
Publisher
Wiley-blackwell
Abstract
Description
Keywords
Turkish CoHE Thesis Center URL
WoS Q
Q1
Scopus Q
Q1
Source
Volume
9
Issue
Start Page
935
End Page
936
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