Role of RNF213 p.4810K variant in the development of intracranial arterial disease in patients treated with nilotinib

J Neurol Sci. 2020 Jan 15:408:116577. doi: 10.1016/j.jns.2019.116577. Epub 2019 Nov 9.
No abstract available

Keywords: Intracranial arterial stenosis; Nilotinib; RNF213.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adenosine Triphosphatases / genetics*
  • Genetic Variation / genetics*
  • Humans
  • Intracranial Arterial Diseases / diagnostic imaging
  • Intracranial Arterial Diseases / drug therapy*
  • Intracranial Arterial Diseases / genetics*
  • Male
  • Middle Aged
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / metabolism
  • Pyrimidines / adverse effects*
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Pyrimidines
  • RNF213 protein, human
  • Ubiquitin-Protein Ligases
  • Protein-Tyrosine Kinases
  • Adenosine Triphosphatases
  • nilotinib