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Case Reports
. 1989 Jul;72(3):452-5.
doi: 10.1111/j.1365-2141.1989.tb07731.x.

Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency

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Case Reports

Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency

S W Eber et al. Br J Haematol. 1989 Jul.

Abstract

We studied the RBC membrane proteins of four patients, including a mother and daughter, with hereditary stomatocytosis. One- and two-dimensional gel electrophoresis revealed that a 28 kDa integral protein, present in normal RBC membranes, was absent in all four patients. This abnormality, reported once previously (Lande et al, 1982), appears to be a characteristic feature of hereditary stomatocytosis, and may be related to the underlying permeability defect in this disorder.

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