Association of the MBL2 gene EXON1 polymorphism and vasoocclusive crisis in patients with sickle cell anemia

Acta Haematologica

Volumn 121, Issue 4, 2009, Pages 212-215

  Oliveira, M C V C ^a   Mendonca T F ^a   Vasconcelos, L R S ^a   Moura, P ^a   Bezerra, M A C ^a   Santos, M N N ^a   Araujo A S ^a   Cavalcanti, M S M ^a  

^a FEDERAL UNIVERSITY OF PERNAMBUCO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

MANNOSE BINDING LECTIN 2;

ARTICLE; BLOOD VESSEL OCCLUSION; DISEASE ASSOCIATION; GENETIC POLYMORPHISM; HUMAN; PATHOGENESIS; PRIORITY JOURNAL; SICKLE CELL ANEMIA; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; ANEMIA, SICKLE CELL; CHILD; CHILD, PRESCHOOL; EXONS; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; ISCHEMIA; MALE; MANNOSE-BINDING LECTIN; POLYMORPHISM, SINGLE NUCLEOTIDE; RECURRENCE; RESPIRATORY TRACT INFECTIONS;

EID: 66049157967     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000220335     Document Type: Article

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