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Autor:
Heul, A.M.B. van der, Nievelstein, R.A., Eijk, R.P.A. van, Asselman, F., Erasmus, C.E., Cuppen, I., Bittermann, A.J., Gerrits, E., Pol, W.Ludo van der, Engel-Hoek, L. van den
Publikováno v:
Journal of Neuromuscular Diseases, 10, 427-438
Journal of Neuromuscular Diseases, 10, 3, pp. 427-438
Journal of Neuromuscular Diseases, 10, 3, pp. 427-438
Item does not contain fulltext BACKGROUND: Spinal muscular atrophy (SMA) is a hereditary motor neuron disorder, characterized by the degeneration of motor neurons and progressive muscle weakness. There is a large variability of disease severity, refl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea7a520a8f5c386b39087df78a7b3c78
https://hdl.handle.net/2066/292707
https://hdl.handle.net/2066/292707
