Functional characterization of a FRMPD4 mutation in a UDP family

Medicine & Life Sciences

1. Undiagnosed Diseases 100%
2. metabotropic glutamate receptor type 1 62%
3. Brain Diseases 41%
4. Epilepsy 36%
5. Mutation 36%
6. Metabotropic Glutamate 5 Receptor 32%
7. Research Personnel 30%
8. Fragile X Syndrome 27%
9. X-Linked Genes 27%
10. Interpersonal Relations 22%
11. Missense Mutation 22%
12. Protein Domains 21%
13. Neuronal Plasticity 20%
14. Intellectual Disability 20%
15. Nervous System Diseases 20%
16. Inborn Genetic Diseases 19%
17. Synapses 19%
18. Transgenic Mice 19%
19. Genes 17%
20. Learning 15%
21. Memory 15%
22. Phosphorylation 14%
23. Neurons 13%
24. Phenotype 12%
25. In Vitro Techniques 9%
26. Proteins 7%
27. Therapeutics 7%