F. T. is a non-paid collaborator with Asuragen, Inc. She has a patent for the detection of FMR1 allele size and category using the CGG linker PCR-based approach. R. H. has received funding for treatment trials in fragile X syndrome or autism from Novartis, Roche, Seaside Therapeutics, Curemark, Forest Pharmaceuticals, and the National Fragile X Foundation. D. H. received support from Novartis, Roche, and Seaside Therapeutics for clinical trials in fragile X syndrome. K. B., R. L., A. S., and C. Y. have no conflicts of interest to disclose.
A family with two female siblings with compound heterozygous FMR1 premutation alleles
Version of Record online: 28 JUL 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 5, pages 458–463, May 2014
How to Cite
Basuta, K., Lozano, R., Schneider, A., Yrigollen, C.M., Hessl, D., Hagerman, R.J. and Tassone, F. (2014), A family with two female siblings with compound heterozygous FMR1 premutation alleles. Clinical Genetics, 85: 458–463. doi: 10.1111/cge.12218
- Issue online: 1 APR 2014
- Version of Record online: 28 JUL 2013
- Accepted manuscript online: 20 JUN 2013 01:02PM EST
- Manuscript Accepted: 18 JUN 2013
- Manuscript Revised: 14 JUN 2013
- Manuscript Received: 5 MAY 2013
- NICHD. Grant Numbers: HD02274, HD036071
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