Artículo
A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2
Registro en:
10.1002/mds.25083
Autor
Perandones, Claudia
Micheli, Federico E
Pellene, Luis A
Bayly, Marta A
Berkovic, Samuel F
Dibbens, Leanne M
Resumen
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.