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    • Partial deficiency of erythrocyte spectrin in hereditary spherocytosis. 

      Bennett, V; McMillan, C; Casella, JF; Asimos, A; Agre, Peter (Nature Publishing Group, 1985-03-28)
      Hereditary spherocytosis (HS) is a common, clinically heterogeneous haemolytic anaemia in which the primary erythrocyte defect is believed to be some abnormality in the spectrin-actin membrane skeleton, leading to loss of ...