Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations

Leukemia Research

Volumn 32, Issue 6, 2008, Pages 972-975

  Okur, Hamza ^a   Balta, Gunay ^a   Akarsu, Nurten ^a   Oner, Ahmet ^b   Patiroglu, Turkan ^c   Bay, Ali ^b   Sayli, Tulin ^d   Unal, Sule ^a   Gurgey, Aytemiz ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

^b YUZUNCU YIL UNIVERSITY   (Turkey)

^c ERCIYES UNIVERSITY   (Turkey)

^d SSK Ankara Diskapi Hospital   (Turkey)

Author keywords

Clinical presentations; FHL; Mutations; Perforin gene

Indexed keywords

PERFORIN;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENE SEQUENCE; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HOMOZYGOSITY; HUMAN; INFANT; LINKAGE ANALYSIS; MALE; MISSENSE MUTATION; NEWBORN; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CODON, NONSENSE; CONSANGUINITY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HOMOZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; LINKAGE (GENETICS); LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC; MALE; MUTATION, MISSENSE; PERFORIN; TURKEY;

EID: 40849097696     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2007.11.033     Document Type: Article

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