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


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

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

  • Publication Type: Article / Letter
  • Volume: 84 Issue: 4
  • Publication Date: 2013
  • Doi Number: 10.1111/cge.12088
  • Title of Journal : CLINICAL GENETICS
  • Page Numbers: pp.394-395