Garbarz M.,1990

Garbarz M., Lecomte M.C., Feo C., Devaux I., Picat C., Lefebvre C., Galibert F., Gautero H., Bournier O., Galand C., Forget B.G., Boivin P., Dhermy D. Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha(I/74) variant related to a CGT to CAT codon change (arg to his) at position 22 of the spectrin alpha-I domain. - Blood, 1990, v. 75, p. 1691-1698.

Смотрите также:

Табл. SPTA m

Табл. SPTB m