Title : Haddad syndrome: a case of an infant with central congenital hypoventilation syndrome and Hirschsprung disease.

Pub. Date : 2008 Mar

PMID : 18230845






1 Functional Relationships(s)
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1 Recent work has associated polyalanine repeats within the PHOX2B gene on chromosome 4p12 with central congenital hypoventilation syndrome, whereas PHOX2B knockout mice develop aganglionic bowels. polyalanine paired-like homeobox 2b Mus musculus