Literature DB >> 12427909

SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist.

P Corcia1, J Khoris, P Couratier, V Mayeux-Portas, E Bieth, B De Toffol, A Autret, J P Müh, C Andres, W Camu.   

Abstract

Spinal muscular atrophy (SMA) is caused by SMN1 gene deletions or mutations, and ALS is the most frequent motor neuron condition in adults. The authors describe three families in which ALS and SMA coexist. The authors found that no SOD1 mutation was found within these families; all three ALS cases had at least two SMN1 copies; and an abnormal SMN1 gene locus did not explain the co-occurrence of these two motor neuron disorders in these families.

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Year:  2002        PMID: 12427909     DOI: 10.1212/01.wnl.0000032500.73621.c5

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.

Authors:  Agnes L Nishimura; Miguel Mitne-Neto; Helga C A Silva; Antônio Richieri-Costa; Susan Middleton; Duilio Cascio; Fernando Kok; João R M Oliveira; Tom Gillingwater; Jeanette Webb; Paul Skehel; Mayana Zatz
Journal:  Am J Hum Genet       Date:  2004-09-15       Impact factor: 11.025

2.  Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies.

Authors:  Shingo Kariya; Diane B Re; Arnaud Jacquier; Katelyn Nelson; Serge Przedborski; Umrao R Monani
Journal:  Hum Mol Genet       Date:  2012-05-11       Impact factor: 6.150

Review 3.  Copy Number Variations in the Survival Motor Neuron Genes: Implications for Spinal Muscular Atrophy and Other Neurodegenerative Diseases.

Authors:  Matthew E R Butchbach
Journal:  Front Mol Biosci       Date:  2016-03-10
  3 in total

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