Please use this identifier to cite or link to this item: http://sgc.anlis.gov.ar/handle/123456789/1577
Title: A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2
Authors: Perandones, Claudia 
Micheli, Federico E 
Pellene, Luis A 
Bayly, Marta A 
Berkovic, Samuel F 
Dibbens, Leanne M 
Keywords: Mutación;Pérdida Auditiva
Issue Date: Aug-2012
Journal: Movement disorders : official journal of the Movement Disorder Society 
URI: http://sgc.anlis.gob.ar/handle/123456789/1577
DOI: 10.1002/mds.25083
Appears in Collections:Publicaciones

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