共 2 条
- [1] HOMOZYGOUS 4.1(-) HEREDITARY ELLIPTOCYTOSIS ASSOCIATED WITH A POINT MUTATION IN THE DOWNSTREAM INITIATION CODON OF PROTEIN-4.1 GENE JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (05): : 1713 - 1717
- [2] 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 JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01): : 77 - 82