A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2

dc.creatorPerandones, Claudia
dc.creatorMicheli, Federico E
dc.creatorPellene, Luis A
dc.creatorBayly, Marta A
dc.creatorBerkovic, Samuel F
dc.creatorDibbens, Leanne M
dc.date2020-05-17T23:01:58Z
dc.date2020-05-17T23:01:58Z
dc.date2012-08
dc.date.accessioned2023-08-29T20:06:50Z
dc.date.available2023-08-29T20:06:50Z
dc.identifierhttp://sgc.anlis.gob.ar/handle/123456789/1577
dc.identifier10.1002/mds.25083
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8519341
dc.descriptionFil: Perandones, Claudia. ANLIS Dr. C. G. Malbrán; Argentina.
dc.descriptionFil: Micheli, Federico E. ANLIS Dr. C. G. Malbrán; Argentina.
dc.descriptionFil: Pellene, Luis A. Universidad de Buenos Aires. Hospital de Clínicas José de San Martín. Programa de Parkinson y Movimientos Anormales; Argentina.
dc.descriptionFil: Bayly, Marta A. University of South Australia. School of Pharmacy and Medical Sciences; Australia.
dc.descriptionFil: Berkovic, Samuel F. University of Melbourne. Epilepsy Research Center and Department of Medicine; Australia.
dc.descriptionFil: Dibbens, Leanne M. University of South Australia. School of Pharmacy and Medical Sciences; Australia.
dc.languageen
dc.relationMovement disorders : official journal of the Movement Disorder Society
dc.rightsnone
dc.subjectMutación
dc.subjectPérdida Auditiva
dc.titleA case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2
dc.typeArtículo


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