Syndromic associations and RNF216 mutations

Parkinsonism Relat Disord. 2015 Nov;21(11):1389-90. doi: 10.1016/j.parkreldis.2015.09.010. Epub 2015 Sep 4.
No abstract available

Keywords: 4H syndrome; Cerebellar ataxia; Hypogonadotropic hypogonadism; RNF216.

Publication types

  • Letter
  • Comment

MeSH terms

  • Cerebellar Ataxia / genetics*
  • Demyelinating Autoimmune Diseases, CNS / genetics*
  • Humans
  • Hypogonadism / genetics*
  • Male
  • Muscle Hypotonia / genetics*
  • Mutation / genetics*
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Ubiquitin-Protein Ligases