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Article

De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype.

Neurology - 17 Sept 2013

Houge Gunnar, Bruland Ove, Bjørnevoll Inga, Hayden Michael R, Semaka Alicia

Abstract excerpt

No abstract is available from the source.

Topics

Female
Genetic Predisposition to Disease
Haplotypes
Humans
Huntington Disease
Middle Aged
Mutation
Pedigree
Risk

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23946314
DOI: 10.1212/WNL.0b013e3182a4a4af
PMCID: PMC3795589

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