dc.creatorGoldemberg, Adriana Lía
dc.creatorMadrid, Enrique Alberto
dc.creatorGarcia, Alicia Mabel
dc.creatorRoubicek, Martín
dc.creatorTrucco, Raúl Esteban
dc.date2013-07-25
dc.date.accessioned2022-11-05T00:49:18Z
dc.date.available2022-11-05T00:49:18Z
dc.identifierhttps://produccioncientificaluz.org/index.php/investigacion/article/view/28345
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5135395
dc.descriptionThe allosteric behaviour of the p-nitrophenyI-phosphatase (E.C.3.1.3.l.) from membrane erythrocytes was investigated in the following multisystemic diseases: myotonic dystrophy, limb-girdle muscular dystrophy. Charcot-Marie-Tooth and juvenile spinal muscular atrophy; in myotonia congenital, which is not a multisystemic disease, and in healthy controls. The Hill coefficient in F-inhibition in controls was different from that in multisystemic diseases patients but not from that in myotonia congenita patients. Changes in the cooperative type kinetics would suggest that the interaction membrane-enzyme in controls and in patients with neuromuscular disorders is onIy different for multisystemic diseases.es-ES
dc.formatapplication/pdf
dc.languagespa
dc.publisherUniversidad del Zuliaes-ES
dc.relationhttps://produccioncientificaluz.org/index.php/investigacion/article/view/28345/29058
dc.rightsDerechos de autor 2016 Investigación Clínicaes-ES
dc.sourceInvestigación Clínica; Vol. 37 Núm. 4es-ES
dc.source2477-9393
dc.source0535-5133
dc.subjectErythrocyte alkaline phosphatasees-ES
dc.subjectmyotonic muscle disorderses-ES
dc.subjectklneticses-ES
dc.subjectinteraction membrane-enzymees-ES
dc.titleErythrocyte alkaline phosphatase in patients with myotonic muscle disorderses-ES
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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