A HomozygousKCNJ10Mutation in Jack Russell Terriers and Related Breeds with Spinocerebellar Ataxia with Myokymia, Seizures, or Both

The MaSuRCA genome assembler

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Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome

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Missense Mutation in CAPN1 Is Associated with Spinocerebellar Ataxia in the Parson Russell Terrier Dog Breed

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Myokymia and neuromyotonia in veterinary medicine: A comparison with peripheral nerve hyperexcitability syndrome in humans

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Experimental validation of in silico predicted KCNA1, KCNA2, KCNA6 and KCNQ2 genes for association studies of peripheral nerve hyperexcitability syndrome in Jack Russell Terriers

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Hereditary ataxia in Jack Russell terriers in the UK

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Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome

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The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel

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Clinical and Electrophysiological Characterization of Myokymia and Neuromyotonia in Jack Russell Terriers

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A method and server for predicting damaging missense mutations

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Inwardly Rectifying Potassium Channels: Their Structure, Function, and Physiological Roles

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Myokymia and neuromyotonia in 37 Jack Russell terriers

(2010) Sofie F. Bhatti et al.   VETERINARY JOURNAL

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations

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Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

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Silencing the Kir4.1 Potassium Channel Subunit in Satellite Glial Cells of the Rat Trigeminal Ganglion Results in Pain-Like Behavior in the Absence of Nerve Injury

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