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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

✍ Scribed by G. MARCHETTI; G. CASTAMAN; M. PINOTTI; B. LUNGHI; M. G. DI IASIO; M. RUGGIERI; F. RODEGHIERO; F. BERNARDI


Book ID
114714166
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
615 KB
Volume
90
Category
Article
ISSN
0007-1048

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