Search

Author/Creator Cilio, M R

1. 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. Issue 5 (30th April 2004)

Authors:
Matera, I; Bachetti, T; Puppo, F; Di Duca, M; Morandi, F; Casiraghi, G M; Cilio, M R; Hennekam, R; Hofstra, R; Schöber, J G; Ravazzolo, R; Ottonello, G; Ceccherini, I
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 5(2004)
Page Start:
373
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗