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Cytomegalovirus gN Genotypes Distribution among Congenitally Infected Newborns and Their Relationship with Symptoms at Birth and Sequelae
Author(s) -
Sara Pignatelli,
Tiziana Lazzarotto,
Maria Rosaria Gatto,
Paola Dal Monte,
Maria Paola Landini,
Giacomo Faldella,
Marcello Lanari
Publication year - 2010
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/653423
Subject(s) - medicine , cytomegalovirus , population , genotype , human cytomegalovirus , cohort , univariate analysis , confidence interval , disease , pediatrics , logistic regression , immunology , multivariate analysis , herpesviridae , viral disease , biology , virus , genetics , environmental health , gene
Cytomegalovirus (CMV) is the leading cause of congenital infection, with morbidity and mortality at birth and sequelae. Both host and viral factors may affect the outcome of infection. CMV strain virulence may depend on genetic variability in "key genes," such as UL73, which encodes the envelope glycoprotein gN. This study aimed to ascertain the role of gN variants as markers of pathogenicity and prognosis in newborns congenitally infected with CMV.

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