respiratory system
|
• abnormal nasal potential difference
|
|
• increased inflammatory response to chronic Pseudomonas aeruginosa infection, identical to that in Cftrtm1Unc homozygotes
|
growth/size
|
• reduced at 14 and 21 days of age relative to wild-type mice
|
digestive/alimentary system
|
• develop intestinal blockage when fed a normal (solid) diet
|
immune system
|
• increased inflammatory response to chronic Pseudomonas aeruginosa infection, identical to that in Cftrtm1Unc homozygotes
|
Mouse Models of Human Disease |
OMIM ID | Ref(s) | |
| Cystic Fibrosis; CF | 219700 | J:112450 | |
