Molecular basis of hemostatic and thrombotic diseases

Author:

Martin Karlyn,Ma Alice D.,Key Nigel S.

Publisher

Elsevier

Reference55 articles.

1. “Summary of Mutations Causing Rare Bleeding Disorders.” International Society on Thrombosis and Haemostasis 2018. Available at https://www.isth.org/general/custom.asp?page=SummaryofMutations. Accessed 11/2/2016.

2. The Human Gene Mutation Database at the Institute of Medial Genetics in Cardiff. Available at http://www.hgmd.cf.ac.uk/ac/index.php. Accessed 11/2/2016.

3. “Glanzmann Thromboasthenia Database.” Medical College of Wisconsin 2016–2018. Available at https://glanzmann.mcw.edu. Accessed 10/16/2019.

4. “Mutations of the Hermansky-Pudlak Syndrome-1 gene (HPS1) associated with Hermansky-Pudlak Syndrome.” International Albinism Center, University of Minnesota. Available at http://www.ifpcs.org/albinism/hps1mut.html. Accessed 10/16/2019.

5. Schaafsma, Gerard. “LYSTbase: Variation registry for Chediak-Higashi syndrome.” ID bases, http://structure.bmc.lu.se/idbase/LYSTbase/index.php?content=index/IDbases. Accessed 10/16/2019.

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