LETTER TO THE EDITOR
Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum
Article first published online: 20 FEB 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 84, Issue 4, pages 394–395, October 2013
How to Cite
A second report of TMCO1 defect syndrome in a patient diagnosed with whole-exome sequencing: expanding phenotypic spectrum., , , , , , , , , , .
- Issue published online: 11 SEP 2013
- Article first published online: 20 FEB 2013
- Accepted manuscript online: 16 JAN 2013 04:10AM EST
- Manuscript Accepted: 29 DEC 2012
- Manuscript Revised: 24 DEC 2012
- Manuscript Received: 15 NOV 2012
- Yale Program on Neurogenetics
- NIH. Grant Number: RC2 NS070477
- Yale Center for Mendelian Disorders. Grant Number: U54HG006504
- Gregory M. Kiez and Mehmet Kutman Foundation
- The Scientific and Technological Research Council of Turkey (TUBITAK)
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