Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians?
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K. Fischbeck | Barrington G. Burnett | S. Traore | S. Doumbia | G. Landouré | M. Sylla | Y. Maiga | S. Coulibaly | K. Meilleur | Y. Coulibaly | C. Guinto | H. Dolo | S. Y. Coulibaly | M. Sangare | I. Dicko | A. Sissoko | K. Dembélé | Y. Coulibaly | A. Diallo | M. Dolo | B. Maiga | M. Traoré | M. Karembé | K. Traoré | A. Touré | A. Togora | B. Hendrickson | Katherine V. Bricceno | A. Schindler | A. Kokkinis | Hammadoun Ali Sangho | B. Diakite | Y. Kassogue | S. Coulibaly | Youlouza Coulibaly | Yaya Ibrahim Coulibaly
[1] A. Singleton,et al. Genetics of low spinal muscular atrophy carrier frequency in sub‐Saharan Africa , 2014, Annals of neurology.
[2] C. Barnes,et al. SMN1 gene duplications are associated with sporadic ALS , 2012, Neurology.
[3] A. Ludolph,et al. Amyotrophic lateral sclerosis. , 2012, Current opinion in neurology.
[4] K. Fischbeck,et al. Genetic testing and counseling for hereditary neurological diseases in Mali , 2011, Journal of Community Genetics.
[5] Y. Hua,et al. A positive modifier of spinal muscular atrophy in the SMN2 gene. , 2009, American journal of human genetics.
[6] T. Scholl,et al. Differences in SMN1 allele frequencies among ethnic groups within North America , 2009, Journal of Medical Genetics.
[7] C. Andres,et al. The importance of the SMN genes in the genetics of sporadic ALS , 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[8] Robert H. Brown,et al. 50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis , 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[9] A. Krause,et al. The molecular basis of Spinal Muscular Atrophy (SMA) in South African black patients , 2007, Neuromuscular Disorders.
[10] K. Sleegers,et al. APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy. , 2006, Brain : a journal of neurology.
[11] B. Giraudeau,et al. SMN1 gene, but not SMN2, is a risk factor for sporadic ALS , 2006, Neurology.
[12] L. H. van den Berg,et al. SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS , 2005, Neurology.
[13] M. A. Alvarez,et al. Evidence of reduced frequency of spinal muscular atrophy type I in the Cuban population , 2005, Neurology.
[14] A Dürr,et al. Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease , 2004, The Lancet.
[15] A Dürr,et al. Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease. , 2004, Lancet.
[16] W. Ewens,et al. Genetic risk assessment in carrier testing for spinal muscular atrophy. , 2002, American journal of medical genetics.
[17] V. Meininger,et al. Deletions causing spinal muscular atrophy do not predispose to amyotrophic lateral sclerosis. , 1999, Archives of neurology.
[18] Robert H. Brown,et al. Amyotrophic lateral sclerosis. Insights from genetics. , 1997, Archives of neurology.
[19] K. Davies,et al. Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy. , 1995, Human molecular genetics.
[20] K. Fischbeck,et al. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. , 1994, Human molecular genetics.
[21] J. Pearn. CLASSIFICATION OF SPINAL MUSCULAR ATROPHIES , 1980, Lancet.
[22] J. Pearn. CLASSIFICATION OF SPINAL MUSCULAR ATROPHIES , 1980, The Lancet.
[23] M. Bjørneboe,et al. KUPFFER CELLS AND CIRRHOSIS , 1975, The Lancet.