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A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2
Claudia Perandones, Federico E. Micheli, Luis A. Pellene, Marta A. Bayly, Samuel F. Berkovic, Leanne M. DibbensVolume:
27
Year:
2012
Language:
english
Pages:
1
DOI:
10.1002/mds.25083
File:
PDF, 192 KB
english, 2012