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Journal Articles

Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self- association site

N Alloisio, R Wilmotte, L Morlé, F Baklouti, J Maréchal, MT Ducluzeau, L Denoroy, C Féo, BG Forget, R Kastally, J Delaunay

Blood (1992) 80 (3): 809–815.

https://doi.org/10.1182/blood.V80.3.809.809

Published: 1992

Journal Articles

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene

F Baklouti, J Maréchal, R Wilmotte, N Alloisio, L Morlé, MT Ducluzeau, L Denoroy, A Mrad, MH Ben Aribia, R Kastally, J Delaunay

Blood (1992) 79 (9): 2464–2470.

https://doi.org/10.1182/blood.V79.9.2464.2464

Published: 1992

Journal Articles

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

L Morle, F Morle, AF Roux, J Godet, BG Forget, L Denoroy, M Garbarz, D Dhermy, R Kastally, J Delaunay

Blood (1989) 74 (2): 828–832.

https://doi.org/10.1182/blood.V74.2.828.828

Published: 1989

Journal Articles

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state

L Morle, N Alloisio, MT Ducluzeau, B Pothier, R Blibech, R Kastally, J Delaunay

Blood (1988) 71 (2): 508–511.

https://doi.org/10.1182/blood.V71.2.508.508

Published: 1988