List of bibliographic references
Number of relevant bibliographic references: 3.
List of associated KwdEn.i
Nombre de documents | Descripteur |
3 | Humans |
2 | Amino Acid Substitution |
2 | Animals |
1 | Adenosine Triphosphate (metabolism) |
1 | Amino Acid Sequence |
1 | Anticonvulsants (therapeutic use) |
1 | Arginine (metabolism) |
1 | Australasia |
1 | Base Sequence |
1 | Binding Sites |
1 | Carrier Proteins (genetics) |
1 | Conserved Sequence |
1 | Disease Models, Animal |
1 | Drug Discovery |
1 | Epilepsy (drug therapy) |
1 | Epilepsy (genetics) |
1 | Epilepsy (pathology) |
1 | Epilepsy, Temporal Lobe (genetics) |
1 | Epilepsy, Temporal Lobe (pathology) |
1 | European Continental Ancestry Group (genetics) |
1 | Exome |
1 | Female |
1 | Gene Expression Regulation (genetics) |
1 | Gene Regulatory Networks (genetics) |
1 | Genes, Dominant |
1 | Genetic Association Studies |
1 | Genetic Predisposition to Disease |
1 | Glutamine (metabolism) |
1 | Heat-Shock Proteins (genetics) |
1 | Male |
1 | Mice |
1 | Models, Molecular |
1 | Molecular Sequence Data |
1 | Multifactorial Inheritance (genetics) |
1 | Multiple Sclerosis (genetics) |
1 | Multiple Sclerosis (metabolism) |
1 | Multiple Sclerosis (pathology) |
1 | Mutation |
1 | Mutation, Missense |
1 | Myoclonic Epilepsies, Progressive (genetics) |
1 | NAV1.1 Voltage-Gated Sodium Channel (genetics) |
1 | Pedigree |
1 | Point Mutation |
1 | Prion Proteins |
1 | Prions (genetics) |
1 | Protein Conformation |
1 | Receptors, Purinergic P2X7 (chemistry) |
1 | Receptors, Purinergic P2X7 (genetics) |
1 | Receptors, Purinergic P2X7 (metabolism) |
1 | Sequence Alignment |
1 | Sequence Homology, Amino Acid |
1 | Shaw Potassium Channels (genetics) |
1 | Shaw Potassium Channels (physiology) |
1 | Species Specificity |
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