Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.
Squitieri F; Gellera C; Cannella M; Mariotti C; Cislaghi G; Rubinsztein DC; Almqvist EW; Turner D; Bachoud-Lévi AC; Simpson SA; Delatycki M; Maglione V; Hayden MR; Donato SD; Brain: A Journal Of Neurology, 2003, vol. 126, issue Pt 4, p 946, ISSN 00068950. ISBN 00068950.

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