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38. Dempsey, J.A. et al . (2010) Pathophysiology of
sleep apnea. Physiol. Rev. 90, 47–112
39. Weese-Mayer, D.E. et al . (2010) An official ATS
clinical policy statement: congenital central
hypoventilation syndrome: genetic basis, diagnosis,
and management. Am. J. Respir. Crit. Care Med.
181, 626–644
40. Garcia, A.J., III et al . (2013) The physiological
determinants of sudden infant death syndrome.
Respir. Physiol Neurobiol. 189, 288–300
41. Carroll, M.S. et al . (2014) Residual chemosensitivity
to ventilatory challenges in genotyped congenital
central hypoventilation syndrome. J. Appl. Physiol.
(1985) 116, 439–450
42. Amiel, J. et al . (2003) Polyalanine expansion and
frameshift mutations of the paired-like homeobox
gene PHOX2B in congenital central hypoventilation
syndrome. Nat. Genet. 33, 459–461
43. Goridis, C. et al . (2010) Phox2b, congenital
central hypoventilation syndrome and the
control of respiration. Semin. Cell Dev. Biol. 21,
814–822
44. Dubreuil, V. et al . (2008) A human mutation in
Phox2b causes lack of CO
2
chemosensitivity, fatal
central apnoea and specific loss of parafacial
neurons. Proc. Natl Acad. Sci. U. S. A. 105, 1067–
1072
45. Rudzinski, E. and Kapur, R.P. (2010) PHOX2B
immunolocalization of the candidate human
retrotrapezoid nucleus. Pediatr. Dev. Pathol. 13,
291–299
46. Levy, J. et al . (2019) Tridimensional mapping of
Phox2b expressing neurons in the brainstem of
adult Macaca fascicularis and identification of the
retrotrapezoid nucleus. J. Comp. Neurol. 527,
2875–2884
47. Perez, I.A. and Keens, T.G. (2013) Peripheral
chemoreceptors in congenital central
hypoventilation syndrome. Respir. Physiol.