Title : Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion.

Pub. Date : 1993 Oct 1

PMID : 8400271






1 Functional Relationships(s)
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1 We detected the in-frame deletion of the trinucleotide CAT, encoding histidine 469, two amino acid residues to the N-terminal side of the abnormal proteolytic cleavage site between residues 470 and 471. Histidine catalase Homo sapiens