Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies
Article first published online: 23 MAY 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 7, pages 1543–1546, July 2013
How to Cite
2013. Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies. Am J Med Genet Part A 161A:1543–1546., , , , , ., ., , , , , , , .
- Issue published online: 19 JUN 2013
- Article first published online: 23 MAY 2013
- Manuscript Accepted: 9 MAR 2013
- Manuscript Received: 4 JAN 2013
- Ministry of Health, Labor and Welfare of Japan
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency
- Ministry of Education, Culture, Sports, Science and Technology
- Takeda Science Foundation
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