Homozygosity for CAG mutation in Huntington
            disease is associated with a more severe clinical course

Please use this identifier to cite or link to this item: http://hdl.handle.net/2328/10785

Title:	Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
Authors:	Turner, David Richard Almqvist, W Bachoud-Levi, A Di Donato, S Cislaghi, G Gellera, C Canella, M Delatycki, M Hayden, Michael R Maglione, V Mariotti, C Simpson, S A Rubinsztein, D Squitieri, F
Issue Date:	2003
Citation:	Squitieri, F., Gellera, C., Canella, M., Mariotti, C., Cislaghi, G., Rubinsztein, D., Almqvist, W., Turner, D.R., Bachoud-Levi, A., Simpson, S.A., et al., 2003. Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course. Brain, 126(4), 946-955.
URI:	http://hdl.handle.net/2328/10785
ISSN:	0006-8950
Appears in Collections:	1109 - Neurosciences

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