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

F Squitieri; C Gellera; M Canella; C Mariotti; G Cislaghi; D Rubinsztein; W Almqvist; David Turner; A Bachoud-Levi; S Simpson; M Delatycki; V Maglione; null Hayden; S Di Donato

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

F Squitieri, C Gellera, M Canella, C Mariotti, G Cislaghi, D Rubinsztein, W Almqvist, David Turner, A Bachoud-Levi, S Simpson, M Delatycki, V Maglione, Hayden, S Di Donato

Research output: Contribution to journal › Article › peer-review

158 Citations (Scopus)

Original language	English
Pages (from-to)	946-955
Number of pages	10
Journal	Brain
Volume	126
Issue number	4
Publication status	Published - 2003

Cite this

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title = "Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course",

author = "F Squitieri and C Gellera and M Canella and C Mariotti and G Cislaghi and D Rubinsztein and W Almqvist and David Turner and A Bachoud-Levi and S Simpson and M Delatycki and V Maglione and Hayden and {Di Donato}, S",

year = "2003",

language = "English",

volume = "126",

pages = "946--955",

journal = "Brain",

issn = "0006-8950",

publisher = "Oxford University Press",

number = "4",

}

TY - JOUR

T1 - Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course

AU - Squitieri, F

AU - Gellera, C

AU - Canella, M

AU - Mariotti, C

AU - Cislaghi, G

AU - Rubinsztein, D

AU - Almqvist, W

AU - Turner, David

AU - Bachoud-Levi, A

AU - Simpson, S

AU - Delatycki, M

AU - Maglione, V

AU - Hayden, null

AU - Di Donato, S

PY - 2003

Y1 - 2003

M3 - Article

SN - 0006-8950

VL - 126

SP - 946

EP - 955

JO - Brain

JF - Brain

IS - 4

ER -