The gliadin-CFTR connection: new perspectives for the treatment of celiac disease
Abstract Familial loss-of-function mutations of the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) channel protein cause cystic fibrosis (CF), the most frequent inherited life-threatening disease in the Caucasian population. A recent study indicates that the gluten/gl...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
BMC,
2019-03-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |