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

---

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)

• 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