LETTER TO THE EDITOR
Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss
Version of Record online: 5 JUL 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 6, pages 592–594, June 2014
How to Cite
Tsurusaki, Y., Yonezawa, R., Furuya, M., Nishimura, G., Pooh, R.K., Nakashima, M., Saitsu, H., Miyake, N., Saito, S. and Matsumoto, N. (2014), Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss. Clinical Genetics, 85: 592–594. doi: 10.1111/cge.12215
- Issue online: 26 APR 2014
- Version of Record online: 5 JUL 2013
- Manuscript Accepted: 9 JUN 2013
- Manuscript Revised: 8 JUN 2013
- Manuscript Received: 8 APR 2013
- Ministry of Health, Labour and Welfare
- Japan Science and Technology Agency
- Strategic Research Program for Brain Sciences
- Ministry of Education, Culture, Sports, Science and Technology of Japan
- Japan Society for the Promotion of Science
- Takeda Science Foundation
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