Publication | Closed Access
Familial defective apolipoprotein B-100: Haplotype analysis of the arginine(3500) → glutamine mutation
36
Citations
27
References
1991
Year
Glutamine MutationAllelic VariantMendelian DisorderAllergyGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyHaplotype AnalysisGenetic FactorMedicineClinical Genetics
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