Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians?

INTRODUCTION: Spinal muscular atrophy (SMA) and sporadic amyotrophic lateral sclerosis (SALS) are both motor neuron disorders. SMA results from the deletion of the survival motor neuron (SMN) 1 gene. High or low SMN1 copy number and the absence of SMN2 have been reported as risk factors for the deve...

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Bibliografische gegevens
Gepubliceerd in:eNeurologicalSci
Hoofdauteurs: Sangare, Modibo, Dicko, Ilo, Guinto, Cheick Oumar, Sissoko, Adama, Dembele, Kekouta, Coulibaly, Youlouza, Coulibaly, Siaka Y., Landoure, Guida, Diallo, Abdallah, Dolo, Mamadou, Dolo, Housseini, Maiga, Boubacar, Traore, Moussa, Karembe, Mamadou, Traore, Kadiatou, Toure, Amadou, Sylla, Mariam, Togora, Arouna, Coulibaly, Souleymane, Traore, Sékou Fantamady, Hendrickson, Brant, Bricceno, Katherine, Schindler, Alice B., Kokkinis, Angela, Meilleur, Katherine G., Sangho, Hammadoun Ali, Diakite, Brehima, Kassogue, Yaya, Coulibaly, Yaya Ibrahim, Burnett, Barrington, Maiga, Youssoufa, Doumbia, Seydou, Fischbeck, Kenneth H.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Elsevier 2016
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Original Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5803066/
https://ncbi.nlm.nih.gov/pubmed/29430530
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ensci.2015.12.001
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