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Journal Articles

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia

S Hayette, D Dhermy, ME dos Santos, M Bozon, D Drenckhahn, N Alloisio, P Texier, J Delaunay, L Morle

Blood (1995) 85 (1): 250–256.

https://doi.org/10.1182/blood.V85.1.250.bloodjournal851250

Published: 1995

Journal Articles

A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sor) [letter]

L Boulanger, D Dhermy, M Garbarz, C Silva, J Randon, R Wilmotte, J Delaunay

Blood (1994) 84 (6): 2056.

https://doi.org/10.1182/blood.V84.6.2056.2056

Published: 1994

Journal Articles

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site

N Parquet, I Devaux, L Boulanger, C Galand, P Boivin, MC Lecomte, D Dhermy, M Garbarz

Blood (1994) 84 (1): 303–308.

https://doi.org/10.1182/blood.V84.1.303.303

Published: 1994

Journal Articles

Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene

M Garbarz, L Boulanger, S Pedroni, MC Lecomte, H Gautero, C Galand, P Boivin, L Feldman, D Dhermy

Blood (1992) 80 (4): 1066–1073.

https://doi.org/10.1182/blood.V80.4.1066.1066

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 Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis

B Pothier, L Morle, N Alloisio, MT Ducluzeau, C Caldani, C Feo, M Garbarz, I Chaveroche, D Dhermy, MC Lecomte

Blood (1987) 69 (6): 1759–1765.

https://doi.org/10.1182/blood.V69.6.1759.1759

Published: 1987

Journal Articles

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

M Garbarz, MC Lecomte, D Dhermy, C Feo, I Chaveroche, H Gautero, O Bournier, C Picat, A Goepp, P Boivin

Blood (1986) 67 (6): 1661–1667.

https://doi.org/10.1182/blood.V67.6.1661.1661

Published: 1986

Journal Articles

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

MC Lecomte, D Dhermy, C Solis, A Ester, C Feo, H Gautero, O Bournier, P Boivin

Blood (1985) 65 (5): 1208–1217.

https://doi.org/10.1182/blood.V65.5.1208.1208

Published: 1985

Journal Articles

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis

M Garbarz, D Dhermy, MC Lecomte, C Feo, I Chaveroche, C Galand, O Bournier, O Bertrand, P Boivin

Blood (1984) 64 (5): 1006–1015.

https://doi.org/10.1182/blood.V64.5.1006.1006

Published: 1984

NARROW

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia

A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sor) [letter]

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site

Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene

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

Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis

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American Society of Hematology

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American Society of Hematology

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