Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glul02Lys) in the second EGF-like domain.

Details

Language :

English

ISSN :

00071048

Volume :

90

Issue :

4

Database :

Complementary Index

Journal :

British Journal of Haematology

Publication Type :

Academic Journal

Accession number :

62732153

Full Text :

https://doi.org/10.1111/j.1365-2141.1995.tb05214.x