Eber S.W.,1996


Eber S.W., Gonzales J.M., Lux M.L., Scarpa A.L., Tse W.T., Dornwell M., Herbers J., Kugler W., Ozcan R., Pekrun A., Gallagher P.G., Scgroter W., Forget B.G., Lux S.E. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. - Nature Genet., 1996, v. 13, p. 214-218.

Смотрите также:

  • Табл. ANK m