Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease.
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K. Pasi | F. Hill | M. D. Williams | A. Guilliatt | C. Toh | M. S. Enayat | P. V. Jenkins | M. Williams | G. Surdhar | M. Enayat | P. Jenkins | M. Williams