Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia - Concepedia

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Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

551

Citations

35

References

1993

Year

Rita Shiang, Stephen G. Ryan, Yazhen Zhu, Angelika F. Hahn, P. O’Connell, John J. Wasmuth

Nature Genetics

Clinical Disordersα1 SubunitNeurobiology Of DiseaseNeurological DisorderInhibitory Glycine ReceptorDominant Neurologic DisorderMolecular BiologyNeurologyNeuroscienceMolecular NeurobiologyNeuropathologyMedicineSynaptic SignalingSocial SciencesNeurogenetics

References

	Year	Citations

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