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Keyword [PRRT2]
Result: 1 - 12 | Page: 1 of 1
1.
PRRT2 Mutants Lead To Glutamate Release And GRIA1 Membrane Surface Distribution Abnormalities
2.
The Characteristics Of PRRT2 Mutation, Genotype-phenotype Correlation Of Paroxysmal Kinesigenic Dyskinesia And Its Potential Mechanisms
3.
Mutation Analysis Of The PRRT2Gene In PRRT2-related Paroxysmal Disorders
4.
Clinical And Molecular Genetic Study Of Paroxysmal Kinesigenic Dyskinesia In Northern Han Chinese
5.
Clinical Observation And Mutation Of PRRT2 Gene In Benign Infantile Epilepsy
6.
Investigation Of The Pathogenicity And Potential Mechanisms Underling PRRT2 Variants
7.
The Establishment Of Patient Specific Induced Pluripotent Stem Cell Models And Animal Models For The Pathogenetic Study Of Paroxysmal Kinesigenic Dyskinesia
8.
PRRT2 Regulates The Molecular Mechanism Of The Release Of Amino Acid Neurotransmitter Vesicles Through The SNARE Complex
9.
Clinical,Genetic And Psychological Features Of Paroxysmal Kinesigenic Dyskinesia
10.
Clinical Features And Molecular Pathogenesis Of Paroxysmal Kinesigenic Dyskinesia
11.
Impact Of Genetic Factors In The Pathogenesis Of Parkinson’s Disease And Paroxysmal Kinesigenic Dyskinesias
12.
Human IPSC-derived 16p11.2 Deletion Neuronal Cells Reveal Haplotype-specific Expression Of MAPK3 Contributing To Variation In Neurodevelopment
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