Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation.
| Autor: | BOYNE, JIM, EVANS, STEVE, POLLITT, RODNEY J., TAYLOR, CHRISTOPHER J., DALTON, ANN |
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| Zdroj: | Journal of Medical Genetics; Jul2000, p543-547, 5p |
| Databáze: | Complementary Index |
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