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Article

No association between the ryanodine receptor 3 gene and autism in a Japanese population.

Psychiatry and clinical neurosciences - 1 Jun 2008

Tochigi Mamoru, Kato Chieko, Ohashi Jun, Koishi Shinko, Kawakubo Yuki, Yamamoto Kenji, Matsumoto Hideo, Hashimoto Ohiko, Kim Soo-Yung, Watanabe Keiichiro, Kano Yukiko, Nanba Eiji, Kato Nobumasa, Sasaki Tsukasa

Abstract excerpt

AIM: Autism is a neurodevelopmental disorder with a complex genetic etiology. Chromosome 15q11-q14 has been proposed to harbor a gene for autism susceptibility because deletion of the region leads to Prader-Willi syndrome or Angelman syndrome, having phenotypic overlap with autism. Here we studie...

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Identifiers

PMID: 18588595
DOI: 10.1111/j.1440-1819.2008.01802.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18588595-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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