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

MATERA I;BACHETTI T;PUPPO F;DI DUCA M;MORANTI F;CASIRAGHI GM;CILIO MR;HENNEKAM R;HOFSTRA R;SCHOBER JG;RAVAZZOLO, ROBERTO;OTTONELLO G;CECCHERINI I.

2004-01-01