Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.

Amyotrophic lateral sclerosis (ALS) is a spontaneous, relentlessly progressive motor neuron disease, usually resulting in death from respiratory failure within 3 years. Variation in the genes SOD1 and TARDBP accounts for a small percentage of cases, and other genes have shown association in both can...

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Váldodahkkit:	Simpson, C, Lemmens, R, Miskiewicz, K, Broom, W, Hansen, V, van Vught, P, Landers, J, Sapp, P, Van Den Bosch, L, Knight, J, Neale, B, Turner, M, Veldink, J, Ophoff, R, Tripathi, V, Beleza, A, Shah, M, Proitsi, P, Van Hoecke, A, Carmeliet, P, Horvitz, H, Leigh, P, Shaw, C, van den Berg, L, Sham, P
Materiálatiipa:	Journal article
Giella:	English
Almmustuhtton:	2009

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.

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