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A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia
Article first published online: 25 OCT 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 86, Issue 3, pages 276–281, September 2014
How to Cite
Roos, L., Fang, M., Dali, C., Jensen, H., Christoffersen, N., Wu, B., Zhang, J., Xu, R., Harris, P., Xu, X., Grønskov, K. and Tümer, Z. (2014), A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia. Clinical Genetics, 86: 276–281. doi: 10.1111/cge.12277
The authors declare no conflicts of interest.
- Issue published online: 20 AUG 2014
- Article first published online: 25 OCT 2013
- Accepted manuscript online: 11 SEP 2013 12:51PM EST
- Manuscript Accepted: 6 SEP 2013
- Manuscript Revised: 5 SEP 2013
- Manuscript Received: 1 AUG 2013
- Shenzhen Municipal Government of China. Grant Number: GJHZ20130417140916986
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