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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 

Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS.

[1]

References

  1. Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS. Weese-Mayer, D.E., Berry-Kravis, E.M., Zhou, L. Am. J. Respir. Crit. Care Med. (2005) [Pubmed]
 
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