A missense mutation in <i>CLIC2</i> associated with intellectual disability is predicted by <i>in silico</i> modeling to affect protein stability and dynamics

Documenti analoghi

• A Missense Mutation in CLIC2 Associated with Intellectual Disability is Predicted by In Silico Modeling to Affect Protein Stability and Dynamics
  di: Witham, Shawn, et al.
  Pubblicazione: (2011)
• An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity
  di: Takano, Kyoko, et al.
  Pubblicazione: (2012)
• An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity
  di: Kyoko Takano, et al.
  Pubblicazione: (2012)
• Novel <i>GNB1</i> missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability
  di: Sofia Steinrücke, et al.
  Pubblicazione: (2016)
• Independent role for presynaptic FMRP revealed by an <i>FMR1</i> missense mutation associated with intellectual disability and seizures
  di: Leila K. Myrick, et al.
  Pubblicazione: (2015)