Esra Dikoglu and Pelin Ozlem Simsek-Kiper these authors contributed equally to this work.
Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome
Version of Record online: 16 AUG 2013
© 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 12, pages 3161–3165, December 2013
How to Cite
2013. Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin Syndrome. Am J Med Genet Part A 161A:3161–3165., , , , , , , .
Conflict of interest: none.
- Issue online: 19 NOV 2013
- Version of Record online: 16 AUG 2013
- Manuscript Accepted: 18 JUL 2013
- Manuscript Received: 29 MAY 2013
- Swiss National Foundation. Grant Number: 310030_132940
- Leenaards Foundation
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