Detection and subtyping of dengue 1-4 and yellow fever viruses by means of a multiplex RT-nested-PCR using degenerated primers

Tropical Medicine and International Health

Volumn 11, Issue 9, 2006, Pages 1432-1441

  Sanchez Seco M P ^a   Rosario, D ^b   Hernandez L ^a   Domingo, C ^a   Valdes K ^b   Guzman M G ^b   Tenorio, A ^a  

^a INSTITUTO DE SALUD CARLOS III   (Spain)

^b INSTITUTO DE MEDICINA TROPICAL PEDRO KOURÍ   (Cuba)

Author keywords

Dengue; Diagnostic; PCR; Yellow fever

Indexed keywords

AGAROSE; VIRUS RNA;

DENGUE FEVER; DISEASE INCIDENCE; GEOGRAPHICAL REGION; MOSQUITO; POLYMERASE CHAIN REACTION; VIRUS;

ANALYTIC METHOD; ARTICLE; CONTROLLED STUDY; DENGUE VIRUS; GENE AMPLIFICATION; GENUS; NONHUMAN; NUCLEOTIDE SEQUENCE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SENSITIVITY AND SPECIFICITY; UNINDEXED SEQUENCE; VALIDATION PROCESS; VIRUS DETECTION; VIRUS TYPING; YELLOW FEVER FLAVIVIRUS;

DENGUE; DENGUE VIRUS; DIAGNOSIS, DIFFERENTIAL; DNA PRIMERS; GENE AMPLIFICATION; GENOME, VIRAL; HUMANS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, VIRAL; SENSITIVITY AND SPECIFICITY; SEQUENCE ALIGNMENT; YELLOW FEVER; YELLOW FEVER VIRUS;

YELLOW FEVER VIRUS GROUP;

EID: 33747888386     PISSN: 13602276     EISSN: 13653156     Source Type: Journal    
DOI: 10.1111/j.1365-3156.2006.01696.x     Document Type: Article

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