The first two cases of MYH9 disorders in Thailand: an international collaborative study

Ann Hematol. 2015 Apr;94(4):707-9. doi: 10.1007/s00277-014-2234-6. Epub 2014 Nov 15.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Child
  • Cytodiagnosis
  • DNA Mutational Analysis
  • Female
  • Hearing Loss, Sensorineural / diagnosis*
  • Hearing Loss, Sensorineural / genetics
  • Hearing Loss, Sensorineural / pathology
  • Humans
  • INDEL Mutation
  • International Cooperation
  • Molecular Motor Proteins / genetics
  • Molecular Sequence Data
  • Myosin Heavy Chains / genetics
  • Thailand
  • Thrombocytopenia / congenital*
  • Thrombocytopenia / diagnosis
  • Thrombocytopenia / genetics
  • Thrombocytopenia / pathology

Substances

  • MYH9 protein, human
  • Molecular Motor Proteins
  • Myosin Heavy Chains

Supplementary concepts

  • MYH9-Related Disorders