Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders

समान संसाधन

• Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
  द्वारा: Hammer, Monia B., और अन्य
  प्रकाशित: (2013)
• SLC25A46 mutations associated with Autosomal Recessive Cerebellar Ataxia in North African families
  द्वारा: Hammer, Monia B., और अन्य
  प्रकाशित: (2017)
• White matter hyperintensities and neurodegenerative dementias
  द्वारा: Sassi, Celeste
  प्रकाशित: (2019)
• Exome Sequencing in Brown-Vialetto-Van Laere Syndrome
  द्वारा: Johnson, Janel O., और अन्य
  प्रकाशित: (2010)
• Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease
  द्वारा: Johnson, Janel O., और अन्य
  प्रकाशित: (2012)