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Autor:
Kristen Zukosky, Manfred Boehm, Andrew B. Singleton, Guibin Chen, Fatoumata N'Go Yaro, Sungyoung Auh, Jonathan H. Nofziger, Mahamadou Traoré, Ke-lian Chen, Rick M. Fairhurst, Alice B. Schindler, Ali Saad, Guida Landouré, Modibo Sangare, Kenneth H. Fischbeck, Barrington G. Burnett, Katherine G. Meilleur, Brant C. Hendrickson, Hee‐Suk Lee, Katherine V. Bricceno, Evgenia Pak, Thomas Scholl, Nouhoum Bocoum, Koumba Bagayogo, Michael P. Fay, Mahamadou Diakite, Abdelbasset Amara, George G. Harmison, Youssoufa Maiga, Hammadoun Ali Sango, Fatoumata Daou, Amalia Dutra, Aldiouma Guindo, Christopher Grunseich, Yaya Ibrahim Coulibaly, Moez Gribaa
Publikováno v:
Annals of Neurology
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 r