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.
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F. Galibert | I. Devaux | C. Féo | M. Lecomte | C. Lefebvre | C. Galand | O. Bournier | M. Garbarz | H. Gautero | C. Picat | C. Lefebvre