Associated Papers
Hereditary platelet function disorder from RASGRP2 gene mutations encoding CalDAG-GEFI identified by whole-exome sequencing in a Korean woman with severe bleeding.
Yun JW et al.
Haematologica, 2019
Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients.
Owaidah T et al.
Npj Genomic Medicine, 2019
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