Cite

    I Matera et al.. “PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome.” Journal of medical genetics, vol. 41, no. 5, 2004, pp. 373–380. http://access.bl.uk/ark:/81055/vdc_100137791730.0x00003f