The Molecular Genetics of Inherited Liver Disease: Asphyxiating Thoracic Dystrophy and Phenotypic Diarrhoea of Infancy

Medicine & Life Sciences

1. Trichohepatoenteric Syndrome 100%
2. Ciliopathies 70%
3. Jeune syndrome 41%
4. Diarrhea 39%
5. Alleles 34%
6. Mutation 33%
7. Blood Platelets 18%
8. Proteins 17%
9. Genes 16%
10. H(+)-K(+)-Exchanging ATPase 12%
11. Sodium-Hydrogen Exchanger 3 12%
12. sodium-iodide symporter 12%
13. Tetratricopeptide Repeat 12%
14. Phenotype 11%
15. Hypopigmentation 11%
16. Sodium-Hydrogen Exchangers 10%
17. Aquaporins 10%
18. Carrier Proteins 10%
19. Enterocytes 9%
20. Microvilli 8%
21. Microsatellite Repeats 8%
22. Adenosine Triphosphatases 7%
23. Microtubules 7%
24. Computational Biology 7%
25. Liver Diseases 6%
26. Single Nucleotide Polymorphism 6%
27. Hepatocytes 6%
28. Ions 6%
29. Epithelial Cells 5%
30. Immunohistochemistry 5%
31. In Vitro Techniques 5%
32. Lipids 5%