Genetics of low spinal muscular atrophy carrier frequency in sub‐Saharan Africa

OBJECTIVE: Spinal muscular atrophy (SMA) is one of the most common severe hereditary diseases of infancy and early childhood in North America, Europe, and Asia. SMA is usually caused by deletions of the survival motor neuron 1 (SMN1) gene. A closely related gene, SMN2, modifies the disease severity....

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Main Authors: Sangaré, Modibo, Hendrickson, Brant, Sango, Hammadoun Ali, Chen, Kelian, Nofziger, Jonathan, Amara, Abdelbasset, Dutra, Amalia, Schindler, Alice B., Guindo, Aldiouma, Traoré, Mahamadou, Harmison, George, Pak, Evgenia, Yaro, Fatoumata N'Go, Bricceno, Katherine, Grunseich, Christopher, Chen, Guibin, Boehm, Manfred, Zukosky, Kristen, Bocoum, Nouhoum, Meilleur, Katherine G., Daou, Fatoumata, Bagayogo, Koumba, Coulibaly, Yaya Ibrahim, Diakité, Mahamadou, Fay, Michael P., Lee, Hee‐Suk, Saad, Ali, Gribaa, Moez, Singleton, Andrew B., Maiga, Youssoufa, Auh, Sungyoung, Landouré, Guida, Fairhurst, Rick M., Burnett, Barrington G., Scholl, Thomas, Fischbeck, Kenneth H.
Format: Artigo
Language:Inglês
Published: Wiley-Liss 2014
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Research Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4112719/
https://ncbi.nlm.nih.gov/pubmed/24515897
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24114
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