Please use this identifier to cite or link to this item: http://sgc.anlis.gob.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 
Description: 
Fil: Perandones, Claudia. ANLIS Dr. C. G. Malbrán; Argentina.

Fil: Micheli, Federico E. ANLIS Dr. C. G. Malbrán; Argentina.

Fil: Pellene, Luis A. Universidad de Buenos Aires. Hospital de Clínicas José de San Martín. Programa de Parkinson y Movimientos Anormales; Argentina.

Fil: Bayly, Marta A. University of South Australia. School of Pharmacy and Medical Sciences; Australia.

Fil: Berkovic, Samuel F. University of Melbourne. Epilepsy Research Center and Department of Medicine; Australia.

Fil: Dibbens, Leanne M. University of South Australia. School of Pharmacy and Medical Sciences; Australia.
URI: http://sgc.anlis.gob.ar/handle/123456789/1577
DOI: 10.1002/mds.25083
Appears in Collections:Publicaciones

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