Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

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Summary

An inversion polymorphism of approximately 900kb on chromosome 17q21, which includes the microtubule‐associated protein tau (MAPT) gene defines two haplotype clades, H1 and H2, which are observed to have a marginally significant excess among patients with Parkinson's disease.

Type
article
Published
2007-08-01
Cited by
167
References
46
Access
Open access

Keywords

Haplotype, Single-nucleotide polymorphism, Odds ratio, Biology, SNP

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