A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants
Author:
Affiliation:
1. Institute of Cardiovascular Sciences, College of Medical and Dental Sciences University of Birmingham Birmingham UK
Funder
Saudi Arabia Cultural Bureau in London
British Heart Foundation
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24114
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5. Characterization of an autosomal dominant bleeding disorder caused by a thrombomodulin mutation. Blood;Dargaud Y.;The Journal of the American Society of Hematology,2015
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