Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia - Concepedia

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Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia

64

Citations

8

References

2004

Year

Maria Kinali, Heinz Jungbluth, L. H. Eunson, Caroline A. Sewry, Adnan Y. Manzur, Eugenio Mercuri, Michael G. Hanna, F. Muntoni

Neuromuscular Disorders

HypertonicityChannelopathiesNeurophysiologyPhysiologySevere NeuromyotoniaProminent Episodic AtaxiaNeuroscienceNeurologyPotassium ChannelopathyNeuropathologyMedicineNeuromusculoskeletal DisorderSocial Sciences

References

	Year	Citations

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