Association of variant alleles of MBL2 gene with vasoocclusive crisis in children with sickle cell anemia.

Mendonça, T F; Oliveira, M C V C; Vasconcelos, L R S; Pereira, L M M B; Moura, P; Bezerra, M A C; Santos, M N N; Araújo, A S; Cavalcanti, M S M

Mendonça, T F; Oliveira, M C V C; Vasconcelos, L R S; Pereira, L M M B; Moura, P; Bezerra, M A C; Santos, M N N; Araújo, A S; Cavalcanti, M S M.

Affiliation

Mendonça TF; Biological Science Institute and College of Medical Sciences, University of Pernambuco, Recife, Brazil.

Blood Cells Mol Dis ; 44(4): 224-8, 2010 Apr 15.

Article in En | MEDLINE | ID: mdl-20172753

Subject(s)

Anemia, Sickle Cell/complications; Mannose-Binding Lectin/genetics; Vascular Diseases/etiology; Alleles; Anemia, Sickle Cell/genetics; Child; Child, Preschool; Exons/genetics; Female; Genetic Predisposition to Disease; Genotype; Haplotypes/genetics; Humans; Infant; Infarction/etiology; Infarction/genetics; Ischemia/etiology; Ischemia/genetics; Male; Mannose-Binding Lectin/physiology; Promoter Regions, Genetic/genetics; Severity of Illness Index; Vascular Diseases/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vascular Diseases / Mannose-Binding Lectin / Anemia, Sickle Cell Type of study: Etiology_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Blood Cells Mol Dis Journal subject: HEMATOLOGIA Year: 2010 Type: Article Affiliation country: Brazil

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