Homogeneous polymerase chain reaction nucleobase quenching assay to detect the 1-kbp deletion in CLN3 that causes Batten disease

Journal of Molecular Diagnostics

Volumn 6, Issue 3, 2004, Pages 260-263

  Rothberg, Paul G ^a   Ramirez Montealegre, Denia ^a   Frazier, Sharon D ^a   Pearce, David A ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; FLUORESCENT DYE; NUCLEIC ACID BASE; PROTEIN CLN3; UNCLASSIFIED DRUG;

ALLELE; AMPLICON; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BASE PAIRING; CHROMOSOME 16; CONTROLLED STUDY; GEL ELECTROPHORESIS; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; MELTING POINT; MOLECULAR PROBE; NEURONAL CEROID LIPOFUSCINOSIS; PATHOGENESIS; POLYMERASE CHAIN REACTION; TEMPERATURE; WILD TYPE;

EID: 4344621683     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1525-1578(10)60519-3     Document Type: Article

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