Molecular basis of hereditary factor VII deficiency in India: five novel mutations including a double missense mutation (Ala191Glu; Trp364Cys) in 11 unrelated patients
Jayandharan, G. R., Viswabandya, A., Nair, S. C., Chandy, M., Srivastava, A.Volume:
92
Langue:
english
Journal:
Haematologica
DOI:
10.3324/haematol.10835
Date:
July, 2007
Fichier:
PDF, 125 KB
english, 2007