Paired-like homeobox gene PHOX2B non-polyalanine repeat expansion mutations: Genotype-phenotype correlation in congenital central hypoventilation syndrome and later onset-CCHS.

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