HTRA2 p.G399S in Parkinson disease, essential tremor, and tremulous cervical dystonia

समान संसाधन

• Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease
  द्वारा: Unal Gulsuner, Hilal, और अन्य
  प्रकाशित: (2014)
• MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing
  द्वारा: Haugarvoll, Kristoffer, और अन्य
  प्रकाशित: (2013)
• No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson’s disease
  द्वारा: Gaare, Johannes J, और अन्य
  प्रकाशित: (2018)
• Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease
  द्वारा: Gaare, Johannes J., और अन्य
  प्रकाशित: (2018)
• Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
  द्वारा: Tzoulis, Charalampos, और अन्य
  प्रकाशित: (2013)