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Article

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population.

Neuroscience research - 1 Sept 2005

Marui Tetsuya, Koishi Shinko, Funatogawa Ikuko, Yamamoto Kenji, Matsumoto Hideo, Hashimoto Ohiko, Nanba Eiji, Kato Chieko, Ishijima Michiko, Watanabe Keiichiro, Kasai Kiyoto, Kato Nobumasa, Sasaki Tsukasa

Abstract excerpt

Autism is a child-onset pervasive developmental disorder, with a significant role of genetic factors in its development. Genome-wide linkage studies have suggested a 7q region as a susceptibility locus for autism. We investigated several single nucleotide polymorphisms (SNPs) of Forkhead Box P2 (FOXP2) and Protein-Tyrosine Phosphatase, Receptor-type, Zeta-1 (PTPRZ1) at the 7q region in Japanese patients with...

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Source

Identifiers

PMID: 15998549
DOI: 10.1016/j.neures.2005.05.003

Genes

FOXP2
PTPRZ1

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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