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Article

From 1997 to 2007: a decade journey through the H1 haplotype on 17q21 chromosome.

Parkinsonism & related disorders - 1 Jan 2009

Kalinderi Kallirhoe, Fidani Liana, Bostantjopoulou Sevasti

Abstract excerpt

The H1 haplotype was first identified 10 years ago. Initially, a dinucleotide polymorphism was detected in the tau (MAPT) gene and was subsequently found to be in linkage disequilibrium (LD) with other polymorphisms, forming the MAPT H1 haplotype, a risk factor for many neurological diseases, considered as tauopathies. Genetic and histopathologic data are in agreement that MAPT and its encoded protein have a...

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Source

Identifiers

PMID: 18424220
DOI: 10.1016/j.parkreldis.2008.03.001

Genes

MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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