Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype–phenotype correlation in congenital central hypoventilation syndrome (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

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