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The gene causing familial hypoalphalipoproteinemia is not caused by a defect in the apo AI-CIII-AIV gene cluster in a Spanish family
Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
An Alu element retroposition in two families with Huntington disease defines a new active Alu subfamily
Differential 3′ polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression
Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat
Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population
(CA)n-dinucleotide repeat at the PDEB locus in 4p16.3
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent
Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease
Cloning and mapping of the α-adducin gene close to D4S95 and assessment of its relationship to Huntington disease
Double-stranded RNA-dependent protein kinase, PKR, binds preferentially to Huntington’s disease (HD) transcripts and is activated in HD tissue
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