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PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalization.

Meng-Han TsaiFang-Shin NianMei-Hsin HsuWei-Szu LiuYo-Tsen LiuChen LiuPo-Hsi LinDaw-Yang HwangYao-Chung ChuangJin-Wu Tsai
Published in: Epilepsia (2019)
PRRT2 missense variants clustering at the C-terminus often lead to protein mislocalization. Failure in protein targeting to the plasma membrane by PRRT2 variants may be a key mechanism in causing PKD and related neurological disorders.
Keyphrases
  • protein protein
  • amino acid
  • intellectual disability
  • gene expression
  • single cell
  • dna methylation
  • rna seq
  • blood brain barrier
  • drug delivery
  • polycystic kidney disease