Mutación SOD1-N19S en una familia de esclerosis lateral amiotrófica. [artículo]
Por: Esteban Pérez, Jesús [Neurología]
| García Redondo, Alberto [Instituto de Investigación i+12].
Colaborador(es): Servicio de Neurología-Neurofisiología | Instituto de Investigación imas12.
Editor: Neurología, 2012Descripción: 27(1):11-5.Recursos en línea: Solicitar documento Resumen: N19S mutation is produced by substitution in the 139 position of SOD1 and was described by Mayeux in a patient with amyotrophic lateral sclerosis (ALS). He suggested that it did not have a causal effect as it was found in asymptomatic and sporadic cases. Other authors in later articles did not agree.
| Tipo de ítem | Ubicación actual | Signatura | Estado | Fecha de vencimiento |
|---|---|---|---|---|
Artículo
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PC9912 (Navegar estantería) | Disponible |
Formato Vancouver:
Vela A, Galán L, Valencia C, Torre P de L, Cuadrado ML, Esteban J,et al. Mutación SOD1-N19S en una familia de esclerosis lateral
amiotrófica. Neurologia. 2012 Jan;27(1):11-5.
PMID: 21549454
Contiene 31 referencias
N19S mutation is produced by substitution in the 139 position of SOD1 and was described by Mayeux in a patient with amyotrophic lateral sclerosis (ALS). He suggested that it did not have a causal effect as it was found in asymptomatic and sporadic cases. Other authors in later articles did not agree.
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