Mutations in human disease
In cooperation with Christer Halldén, Christina Lind-Hallden, both at HKR, and Stefan Lethagen at Novo-Nordisk/Rigshospitalet Köpenhamn with coworkers, I am involved in an analysis of inherited coagulation disorders. We have identified a series of deletion relating to Protein S deficiency and recently analyzed a Swedish cohort of patients with Type 1 von Willebrand’s Disease. At present we are working on the last disease with a larger sample of patients from all over Europe.
Page Manager: Martin Stervander
Questions about the website: Web group
Publisher: Department of Biology
Last modified 5 Sep 2011
People involved
Collaborators
Christer Halldén, HKR Christina Lind-Halldén, HKR Stefan Lethagen, Copenhagen University Hospital
Lund University, Box 117, SE-221 00 Lund, Sweden. Tel: +46 (0)46 222 00 00