Leukodystrophy without Ovarian Failure Caused by Compound Heterozygous Alanyl-tRNA Synthetase 2 Mutations

Chin Med J (Engl). 2017 Dec 20;130(24):3021-3022. doi: 10.4103/0366-6999.220300.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Alanine-tRNA Ligase / genetics*
  • Amino Acid Sequence
  • Demyelinating Diseases / genetics*
  • Female
  • Humans
  • Mutation*
  • Ovarian Diseases

Substances

  • Alanine-tRNA Ligase