Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum


Creative Commons License

ÇAĞLAYAN A. O., PER H., Akgumus G., GÜMÜŞ H., Baranoski J., CANPOLAT M., ...More

CLINICAL GENETICS, vol.84, no.4, pp.394-395, 2013 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Letter
  • Volume: 84 Issue: 4
  • Publication Date: 2013
  • Doi Number: 10.1111/cge.12088
  • Journal Name: CLINICAL GENETICS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.394-395
  • Dokuz Eylül University Affiliated: No