Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene
Article first published online: 16 SEP 2008
©2008 The Author(s)/Journal Compilation ©2008 Foundation Acta Pædiatrica/Acta Pædiatrica
Volume 98, Issue 1, pages 192–195, January 2009
How to Cite
Repetto, G. M., Corrales, R. J., Abara, S. G., Zhou, L., Berry-Kravis, E. M., Rand, C. M. and Weese-Mayer, D. E. (2009), Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene. Acta Paediatrica, 98: 192–195. doi: 10.1111/j.1651-2227.2008.01039.x
- Issue published online: 9 DEC 2008
- Article first published online: 16 SEP 2008
- Received 10 June 2008; revised 16 August 2008; accepted 25 August 2008.
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