Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion
Copyright policy )Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion
Frontotemporal dementia (FTD) as an important clinical entity was rediscovered in Lund and Manchester in the early 1990s. Here we show that the large Lund pedigree with behavioral variant of frontotemporal dementia previously described with this disorder has an expansion in the recently described C9ORF72 locus on chromosome 9.
- UCL INSTITUTE OF NEUROLOGY United Kingdom
- UCL Queen Square Institute of Neurology United Kingdom
- National Institute of Health Pakistan
- National Institutes of Health United States
- National Institute on Aging United States
Genetic Markers, Sweden, C9orf72 Protein, Genetic Variation, Proteins, Polymorphism, Single Nucleotide, Pedigree, Risk Factors, Prevalence, Humans, Genetic Predisposition to Disease, Frontotemporal Lobar Degeneration, Repetitive Sequences, Nucleic Acid
Genetic Markers, Sweden, C9orf72 Protein, Genetic Variation, Proteins, Polymorphism, Single Nucleotide, Pedigree, Risk Factors, Prevalence, Humans, Genetic Predisposition to Disease, Frontotemporal Lobar Degeneration, Repetitive Sequences, Nucleic Acid
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