A novel heterozygous SETX mutation in a patient presenting with chorea and motor neuron disease.

Autor: Saracchi, Enrico1 (AUTHOR), Castelli, Marianna2 (AUTHOR), Bassi, Maria T.2 (AUTHOR), Brighina, Erika3 (AUTHOR), Cereda, Diletta1 (AUTHOR), Marzorati, Laura1 (AUTHOR), Patassini, Mirko4 (AUTHOR), Appollonio, Ildebrando1 (AUTHOR), Ferrarese, Carlo1 (AUTHOR), Brighina, Laura1 (AUTHOR) brighinalaura@hotmail.com
Zdroj: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Mar2014, Vol. 15 Issue 1/2, p138-140. 3p.
Databáze: Academic Search Ultimate
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