Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: Detection of a new polymorphic mutation

Annals of Human Genetics

Volumn 63, Issue 3, 1999, Pages 193-197

  Simonsen, K ^a   Dissing, J ^b   Rudbeck, L ^b   Schwartz, M ^c  

^a ROSKILDE HOSPITAL   (Denmark)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

^c University of Copenhagen   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE; CYSTEINE; IRON; SERINE; THYMINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; BLOOD DONOR; CODON; DENMARK; EUROPE; GENE FREQUENCY; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; GENETIC POLYMORPHISM; GENETIC SCREENING; HEMOCHROMATOSIS; HUMAN; HUMAN CELL; MISSENSE MUTATION; NORMAL HUMAN; NUCLEIC ACID BASE SUBSTITUTION; POLYMERASE CHAIN REACTION; POPULATION GENETICS; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADOLESCENT; ADULT; ALLELES; AMINO ACID SUBSTITUTION; CHILD; CHILD, PRESCHOOL; DNA; DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENETIC SCREENING; HEMOCHROMATOSIS; HUMANS; INFANT; MUTATION; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

STAPHYLOCOCCUS PHAGE 187;

EID: 0032845794     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480099007459     Document Type: Article

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