Molecular bases of CRM+ factor X deficiency: a frequent...

British Journal of Haematology 1995 Vol. 90; Iss. 4

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

G. MARCHETTI, G. CASTAMAN, M. PINOTTI, B. LUNGHI, M. G. DI IASIO, M. RUGGIERI, F. RODEGHIERO, F. BERNARDI
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Volume:
90
Year:
1995
Language:
english
Pages:
6
DOI:
10.1111/j.1365-2141.1995.tb05214.x
File:
PDF, 615 KB
english, 1995
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