Coinheritance of two α-spectrin gene defects in a recessive spherocytosis family

Clinical and Laboratory Haematology

Volumn 22, Issue 6, 2000, Pages 329-336

  Dhermy, D ^a,d   Steen Johnsen, J ^b   Bournier, O ^c   Hetet, G ^b,c   Cynober, T ^c,d   Tchernia, G ^c,d   Grandchamp, B ^a  

^a Dept Child/Adolescent Psychiatry   (Norway)

^b BICHAT HOSPITAL   (France)

^c BICÊTRE HOSPITAL   (France)

^d INSERM   (France)

Author keywords

spectrin Bughill; spectrin LEPRA; Haplotyping; Recessive hereditary spherocytosis

Indexed keywords

COMPLEMENTARY DNA; FODRIN; MESSENGER RNA;

ALLELISM; ARTICLE; CLINICAL ARTICLE; DINUCLEOTIDE REPEAT; GENE AMPLIFICATION; GENE EXPRESSION; GENETIC POLYMORPHISM; HAPLOTYPE; HEREDITARY SPHEROCYTOSIS; HUMAN; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; RECESSIVE INHERITANCE; RNA TRANSLATION;

ANEMIA; CHILD, PRESCHOOL; DISEASES IN TWINS; EXCHANGE TRANSFUSION, WHOLE BLOOD; FEMALE; GENES, RECESSIVE; HUMANS; HYPERBILIRUBINEMIA; INFANT; MALE; PEDIGREE; PHOTOTHERAPY; SPECTRIN; SPHEROCYTOSIS, HEREDITARY; TWINS, DIZYGOTIC;

EID: 0034454779     PISSN: 01419854     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2257.2000.00319.x     Document Type: Article

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