Okamoto Y.,1996


Okamoto Y., Yamazaki T., Katsumi A., Kojima T., Takamatsu J., Nishida M., Saito H. A novel nonsense mutation associated with an exon skipping in a patient with hereditary protein S deficiency type I. - Thromb.Haemost., 1996, v. 75, p. 877-882.

Смотрите также:

  • Табл. S m