Novel Rare Missense Variations and Risk of Autism Spectrum Disorder: Whole-Exome Sequencing in Two Families with Affected Siblings and a Two-Stage Follow-Up Study in a Japanese Population

Lignende værker

• Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population
  af: Inoue, Emiko, et al.
  Udgivet: (2015)
• PM338. Investigation of the association of rare single nucleotide variants in methyl-CpG-binding domain protein 5 (MBD5) with phenotypes of autism spectrum disorders and schizophrenia.
  af: Ishizuka, Kanako, et al.
  Udgivet: (2016)
• The lowest effective plasma concentration of atomoxetine in pediatric patients with attention deficit/hyperactivity disorder: A non-randomized prospective interventional study
  af: Sugimoto, Atsunori, et al.
  Udgivet: (2021)
• Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study
  af: Igeta, Hirofumi, et al.
  Udgivet: (2019)
• Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.
  af: Kanako Ishizuka, et al.
  Udgivet: (2016-01-01)