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Your search keyword '"Claudia Perandones"' showing total 2 results
Start Over Author "Claudia Perandones" Journal movement disorders
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2. A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2

Author

Samuel F. Berkovic, Leanne M. Dibbens, Luis A. Pellene, Federico Micheli, Marta A. Bayly, and Claudia Perandones

Subjects
medicine.medical_specialty, Action Myoclonus Renal Failure Syndrome, medicine.diagnostic_test, Pure tone, Hearing loss, business.industry, SCARB2, Severe hearing loss, Audiology, Neurology, Internal medicine, Mutation (genetic algorithm), medicine, Cardiology, Auditory pathways, Neurology (clinical), medicine.symptom, Audiometry, business
Published
2012

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