Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function

Annabel Maclachlan, Steve Watson, Neil Morgan, Gerry Dolan, Charlotte Grimley

Research output: Contribution to journal › Article › peer-review

7 Citations (Scopus)
156 Downloads (Pure)

Fingerprint

Dive into the research topics of 'Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function'. Together they form a unique fingerprint.

Medicine & Life Sciences