Literature DB >> 21247266

A novel L67P SOD1 mutation in an Italian ALS patient.

Alessandra del Grande1, Marco Luigetti, Amelia Conte, Irene Mancuso, Serena Lattante, Giuseppe Marangi, Giuseppe Stipa, Marcella Zollino, Mario Sabatelli.   

Abstract

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting motor neurons. We describe a novel L67P mutation located in exon 3 of the Cu/Zn superoxide dismutase gene in a patient with pure lower motor neuron signs. To date, 11 mutations involving exon 3 of SOD1 have been described, including the present one. Our data confirm that variable penetrance and predominant lower motor neuron involvement are common characteristics in patients bearing mutations in exon 3 of the SOD1 gene.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21247266     DOI: 10.3109/17482968.2011.551939

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  2 in total

1.  Evolutionary Analyses of Sequence and Structure Space Unravel the Structural Facets of SOD1.

Authors:  Sourav Chowdhury; Dwipanjan Sanyal; Sagnik Sen; Vladimir N Uversky; Ujjwal Maulik; Krishnananda Chattopadhyay
Journal:  Biomolecules       Date:  2019-12-04

2.  Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort.

Authors:  Stefania Scarlino; Teuta Domi; Laura Pozzi; Alessandro Romano; Giovanni Battista Pipitone; Yuri Matteo Falzone; Lorena Mosca; Silvana Penco; Christian Lunetta; Valeria Sansone; Lucio Tremolizzo; Raffaella Fazio; Federica Agosta; Massimo Filippi; Paola Carrera; Nilo Riva; Angelo Quattrini
Journal:  Int J Mol Sci       Date:  2020-05-08       Impact factor: 5.923

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.