An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells (Q24618310)
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Current Data About An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells
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(P1476) "An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells" (language: en)

(P2093) J G Conboy
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J A Chasis
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R Winardi
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G Tchernia
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Y W Kan
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N Mohandas
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External Links
(P356) 10.1172/JCI116203
(P698) 8423235
(P932) 329997
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