Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: Application to aspartylglucosaminuria in Finland

Genomics

Volumn 12, Issue 3, 1992, Pages 590-595

  Syvänen, Ann Christine ^a   Ikonen, Elina ^a   Manninen, Tuula ^a   Bengtström, Marina ^b   Söderlund, Hans ^b   Aula, Pertti ^c   Peltonen, Leena ^a  

^a NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^b ORION CORPORATION   (Finland)

^c UNIVERSITY OF TURKU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ASPARTYLGLYCOSAMINURIA; CONTROLLED STUDY; DNA SEQUENCE; FINLAND; GENE FREQUENCY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MUTATION; NORMAL HUMAN; POPULATION GENETICS;

ACETYLGLUCOSAMINE; ALLELES; ASPARTYLGLUCOSYLAMINASE; BASE SEQUENCE; DNA; FINLAND; GENE FREQUENCY; GENETIC TECHNIQUES; HETEROZYGOTE DETECTION; HUMAN; LEUKOCYTES; LYSOSOMAL STORAGE DISEASES; MOLECULAR SEQUENCE DATA; MUTATION; OLIGODEOXYRIBONUCLEOTIDES; POLYMERASE CHAIN REACTION; PREVALENCE; SUPPORT, NON-U.S. GOV'T;

EID: 0026578477     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/0888-7543(92)90452-X     Document Type: Article

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