Correction: Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

Схожие документы

• Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort
  по: Zhang, Qingping, et al.
  Опубликовано: (2018)
• Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
  по: Zhang, Qingping, et al.
  Опубликовано: (2017)
• Rett and Rett‐like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene
  по: Wang, Jiaping, et al.
  Опубликовано: (2019)
• Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation
  по: Wang, Jiaping, et al.
  Опубликовано: (2018)
• SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures
  по: Wang, Jiaping, et al.
  Опубликовано: (2017)