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Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis

✍ Scribed by D. Dhermy; M. Garbarz; Marie-Christine Lecomte; Isabelle Chaveroche; Odile Bournier; Huguette Gautero; Isa Blot; P. Boivin


Book ID
104701784
Publisher
Springer
Year
1986
Tongue
English
Weight
564 KB
Volume
74
Category
Article
ISSN
0340-6717

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Spectrin modifications in a heterozygous
✍ Dr. Sara Streichman; Ethy Herz; Ilana Tatarsky πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 504 KB

The clinical and hematological parameters of a patient described here, who inherited the genes of both hereditary elliptocytosis (HE) and p-thalassemia, seem to reflect a mutual enhancement of the two diseases. The coexistence of the two pathologies is probably also responsible for the observed chan