Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.

Journal of medical genetics

Volumn 43, Issue 4, 2006, Pages

  Rudd, E ^a   Goransdotter Ericson K ^a   Zheng, C ^a   Uysal, Z ^a   Ozkan, A ^a   Gurgey A ^a   Fadeel, B ^a   Nordenskjold M ^a   Henter, J I ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

SYNTAXIN;

ACUTE DISEASE; ADULT; AGED; CHILD; FEMALE; GENETICS; GENOTYPE; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HUMAN; INFANT; LETTER; MALE; MUTATION; MYELODYSPLASTIC SYNDROME; MYELOID LEUKEMIA; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD; PSYCHOMOTOR DISORDER; REMISSION;

ACUTE DISEASE; ADULT; AGED, 80 AND OVER; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; INFANT; LEUKEMIA, MYELOID; LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC; MALE; MUTATION; MYELODYSPLASTIC SYNDROMES; PEDIGREE; PHENOTYPE; PSYCHOMOTOR DISORDERS; QA-SNARE PROTEINS; REMISSION, SPONTANEOUS;

MLCS; MLOWN;

EID: 33745052933     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2005.035253     Document Type: Letter

References (0)