DOI:
10.1055/s-00000059
Pneumologie
LinksClose Window
References
Amiel J, Laudier B, Attié-Bitach T. et al.
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.
Nat Genet 2003;
33: 459-461
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.