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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. [electronic resource] by
- 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
Producer: 20040716
In:
Journal of medical genetics vol. 41
Availability: No items available.
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