Paired-like homeobox gene PHOX2B non-polyalanine repeat expansion mutations: Genotype-phenotype correlation in congenital central hypoventilation syndrome and later onset-CCHS.
Speakers: Amy Zhou; Casey M. Rand; Sara M. Hockney; Grace Niewijk; Patrick Reineke; Virginia Speare; Elizabeth M. Berry-Kravis; Lili Zhou; Lawrence J. Jennings; Min Yu; Isabella Ceccherini; Tiziana Bachetti; Melanie Pennock; Kai Lee Yap; Debra E. Weese-Mayer
Collaborators: Ann & Robert H. Lurie Children's Hospital; IRCCS Istituto Giannina Gaslini; Northwestern University Feinberg School of Medicine; Rush University Medical Center