Matera, I., Bachetti, T., Puppo, F., Di, D., Morandi, F., Casiraghi, G., . . . Ceccherini, I. (2004). 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. BMJ Group.
Citação norma ChicagoMatera, I., 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. BMJ Group, 2004.
Citação norma MLAMatera, I., 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. BMJ Group, 2004.