No association between the ryanodine receptor 3 gene and autism in a Japanese population - 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; et al. (Psychiatry and clinical neurosciences, 2008)
Keywords: Adolescent; Adult; Alleles; association study; autism; Autistic Disorder - genetics; Biological and medical sciences; Child; Child clinical studies; chromosome 15; Chromosomes, Human, Pair 15 - genetics; Developmental disorders; Female; Gene Frequency - genetics; Genetic Predisposition to Disease - genetics; Genetics, Population; Genotype; Humans; Infantile autism; Japan; Linkage Disequilibrium - genetics; Male; Medical sciences; Phenotype; Polymorphism, Single Nucleotide - genetics; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; ryanodine receptor; Ryanodine Receptor Calcium Release Channel - genetics; single nucleotide polymorphism; Japan; Autism; Gene; Ryanodine receptor; association study; Genetics; Developmental disorder; Single nucleotide polymorphism; Genetic determinism; Japanese; chromosome 15