Communicated by Reed E. Pyeritz
Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype of FKBP10 Mutations
Version of Record online: 8 JUL 2013
PUBLISHED 2013. THIS ARTICLE HAS BEEN CONTRIBUTED TO BY US GOVERNMENT EMPLOYEES AND THEIR WORK IS IN THE PUBLIC DOMAIN IN THE USA.
Volume 34, Issue 9, pages 1279–1288, September 2013
How to Cite
Barnes, A. M., Duncan, G., Weis, M., Paton, W., Cabral, W. A., Mertz, E. L., Makareeva, E., Gambello, M. J., Lacbawan, F. L., Leikin, S., Fertala, A., Eyre, D. R., Bale, S. J. and Marini, J. C. (2013), Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype of FKBP10 Mutations. Hum. Mutat., 34: 1279–1288. doi: 10.1002/humu.22362
Contract grant sponsors: NICHD; NIAMS; NIH (HD22657, AR37694, AR37318, AR061118, and AR048544).
- Issue online: 14 AUG 2013
- Version of Record online: 8 JUL 2013
- Accepted manuscript online: 25 MAY 2013 05:26AM EST
- Manuscript Accepted: 16 MAY 2013
- Manuscript Received: 18 MAR 2013
- NIH. Grant Numbers: HD22657, AR37694, AR37318, AR061118, AR048544
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