The 782C → T (T254M) XHIM mutation: Lack of a tight phenotype-genotype relationship [8] (multiple letters)

Blood

Volumn 94, Issue 4, 1999, Pages 1488-1490

  De Vries, E ^a   Noordzij, J G ^a   Davies, E G ^a   Hartwig, N ^a   Breuning, M H ^a   Van Dongen, J J M ^a   Van Tol, M J D ^a   Ochs, H D ^a   Seyama, K ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL ARTICLE; GENE MUTATION; GENOTYPE; HUMAN; HYPERIMMUNOGLOBULINEMIA; HYPERIMMUNOGLOBULINEMIA M; LETTER; PHENOTYPE; PRIORITY JOURNAL; ADULT; CASE REPORT; CHILD; FEMALE; GENETIC LINKAGE; GENETICS; HYPERGAMMAGLOBULINEMIA; IMMUNOLOGY; MALE; NOTE; PEDIGREE; POINT MUTATION; PRESCHOOL CHILD; X CHROMOSOME;

CD40 LIGAND; IMMUNOGLOBULIN M; MEMBRANE PROTEIN;

ADULT; CD40 LIGAND; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; HYPERGAMMAGLOBULINEMIA; IMMUNOGLOBULIN M; LINKAGE (GENETICS); MALE; MEMBRANE GLYCOPROTEINS; PEDIGREE; POINT MUTATION; X CHROMOSOME;

EID: 0033566416     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v94.4.1488     Document Type: Letter

References (0)