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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

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain

M Garbarz, MC Lecomte, C Feo, I Devaux, C Picat, C Lefebvre, F Galibert, H Gautero, O Bournier, C Galand

Blood (1990) 75 (8): 1691–1698.

https://doi.org/10.1182/blood.V75.8.1691.1691

Published: 1990

Journal Articles

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes

MC Lecomte, M Garbarz, B Grandchamp, C Feo, H Gautero, I Devaux, O Bournier, C Galand, L d'Auriol, F Galibert

Blood (1989) 74 (3): 1126–1133.

https://doi.org/10.1182/blood.V74.3.1126.1126

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

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

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes

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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