Correction: Long-read trio sequencing of individuals with unsolved intellectual disability

類似資料

• Long-read trio sequencing of individuals with unsolved intellectual disability
  著者:: Pauper, Marc, 等
  出版事項: (2020)
• TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function
  著者:: Ba, Wei, 等
  出版事項: (2016)
• Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation
  著者:: Acuna-Hidalgo, Rocio, 等
  出版事項: (2015)
• Mutations specific to the Rac-GEF domain of TRIO cause intellectual disability and microcephaly
  著者:: Pengelly, Reuben J, 等
  出版事項: (2016)
• Syndromic X-linked intellectual disability segregating with a missense variant in RLIM
  著者:: Tønne, Elin, 等
  出版事項: (2015)