Défauts génétiques du contrôle de l'activation T évoluant vers un syndrome d'activation lymphohistiocytaire

Archives de Pediatrie

Volumn 6, Issue SUPPL.2, 1999, Pages 417-419

  Dufourcq Lagelouse, R ^a   Pastural, E ^a   Barrat, F J ^a   Le Deist, F ^a   Fischer, A ^a   De Saint Basile, G ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHEDIAK HIGASHI SYNDROME; CHROMOSOME MAP; GENETIC LINKAGE; GENETICS; HISTIOCYTOSIS; HUMAN; IMMUNE DEFICIENCY; IMMUNOLOGY; LYMPHOCYTE ACTIVATION; SYNDROME; T LYMPHOCYTE;

CHEDIAK-HIGASHI SYNDROME; CHROMOSOME MAPPING; HISTIOCYTOSIS, NON-LANGERHANS-CELL; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; LINKAGE (GENETICS); LYMPHOCYTE ACTIVATION; SYNDROME; T-LYMPHOCYTES;

EID: 0038239229     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0929-693x(99)80487-4     Document Type: Article

References (7)

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2. Barrat FJ, Auloge L, Pastural E, Dufourcq-Lagelouse R, Vilmer E, Cant AJ, et al. Genetic and physical mapping of the Chediak-Higashi syndrome on Chr 1q42-43. Am J Hum Genet 1996 ; 59 : 625-32.
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