Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population

Journal of Inherited Metabolic Disease

Volumn 33, Issue 1, 2010, Pages 33-42

  Coffee, Erin M ^a   Yerkes, Laura ^b   Ewen, Elizabeth P ^a   Zee, Tiffany ^b,c   Tolan, Dean R ^a,b  

^a Boston University   (United States)

^b BOSTON UNIVERSITY   (United States)

^c NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; FRUCTOSE BISPHOSPHATE ALDOLASE;

ARTICLE; CONTROLLED STUDY; DNA ISOLATION; GENE AMPLIFICATION; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC SCREENING; GENOTYPE; HEREDITARY FRUCTOSE INTOLERANCE; HOMOZYGOSITY; HUMAN; HYBRIDIZATION; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTANT; NONSENSE MUTATION; NULL ALLELE; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; PREVALENCE; SYMPTOM; UNITED STATES;

ALLELES; BIOPSY; DNA; DNA PRIMERS; FRUCTOSE INTOLERANCE; FRUCTOSE-BISPHOSPHATE ALDOLASE; GENOTYPE; HUMANS; LIVER; MUTATION; MUTATION, MISSENSE; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDES; PREVALENCE; UNITED STATES;

EID: 77649234518     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-009-9008-7     Document Type: Article

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