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Article

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.

Human genetics - 1 Apr 2004

Peyrard-Janvid Myriam, Anthoni Heidi, Onkamo Päivi, Lahermo Päivi, Zucchelli Marco, Kaminen Nina, Hannula-Jouppi Katariina, Nopola-Hemmi Jaana, Voutilainen Arja, Lyytinen Heikki, Kere Juha

Abstract excerpt

Developmental dyslexia, or reading disability, is a multigenic complex disease for which at least five loci, i.e. DYX1-3 and DYX5-6, have been clearly identified from the human genome. To date, DYX1C1 is the only dyslexia candidate gene cloned. We have previously reported linkage to 2p11 and 7q32 in 11 Finnish pedigrees. Here, we report the fine mapping of the approximately 40-cM linked region from chromosome 2...

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Source

Identifiers

PMID: 15007729
DOI: 10.1007/s00439-004-1103-0

Genes

TACR1
NPL

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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