8csw
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Local refinement of protein 4.2 in Class 2 of erythrocyte ankyrin-1 complex
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Structural highlights
DiseaseEPB42_HUMAN Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry. FunctionEPB42_HUMAN Probably plays an important role in the regulation of erythrocyte shape and mechanical properties. Contents | ||||||||||||||||||
This page was last modified 09:40, 14 February 2024.