PHOXs
Paired-like homeobox domain proteins
Members
PHOX2B (MIM.603851) (4p12) (mutations in congenital central hypoventilation syndrome (MIM.209880) and short-segment Hirschsprung disease
Members
PHOX2B (MIM.603851) (4p12) (mutations in congenital central hypoventilation syndrome (MIM.209880) and short-segment Hirschsprung disease
Copyright www.humpath.com, website in human pathology | Web design by PBCom.net