A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
706-720
Beck, J.
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Rohrer, J.D.
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Campbell, T.
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Isaacs, A.
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Morrison, K.E.
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Goodall, E.F.
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Warrington, E.K.
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Stevens, J.
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Revesz, T.
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Holton, J.
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Al-Sarraj, S.
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King, A.
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Scahill, R.
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Warren, J.D.
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Fox, N.C.
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Rossor, M.N.
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Collinge, J.
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Mead, S.
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March 2008
Beck, J.
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Rohrer, J.D.
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Campbell, T.
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Isaacs, A.
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Morrison, K.E.
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Goodall, E.F.
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Warrington, E.K.
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Stevens, J.
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Revesz, T.
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Holton, J.
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Al-Sarraj, S.
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King, A.
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Scahill, R.
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Warren, J.D.
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Fox, N.C.
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Rossor, M.N.
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Collinge, J.
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Mead, S.
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Beck, J., Rohrer, J.D., Campbell, T., Isaacs, A., Morrison, K.E., Goodall, E.F., Warrington, E.K., Stevens, J., Revesz, T., Holton, J., Al-Sarraj, S., King, A., Scahill, R., Warren, J.D., Fox, N.C., Rossor, M.N., Collinge, J. and Mead, S.
(2008)
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.
Brain, 131 (3), .
(doi:10.1093/brain/awm320).
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Accepted/In Press date: 11 December 2007
e-pub ahead of print date: 29 January 2008
Published date: March 2008
Organisations:
Medical Education
Identifiers
Local EPrints ID: 398777
URI: http://eprints.soton.ac.uk/id/eprint/398777
ISSN: 0006-8950
PURE UUID: f407230c-221c-4c80-9d37-03b662bc9513
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Date deposited: 02 Aug 2016 10:27
Last modified: 15 Mar 2024 01:41
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Contributors
Author:
J. Beck
Author:
J.D. Rohrer
Author:
T. Campbell
Author:
A. Isaacs
Author:
K.E. Morrison
Author:
E.F. Goodall
Author:
E.K. Warrington
Author:
J. Stevens
Author:
T. Revesz
Author:
J. Holton
Author:
S. Al-Sarraj
Author:
A. King
Author:
R. Scahill
Author:
J.D. Warren
Author:
N.C. Fox
Author:
M.N. Rossor
Author:
J. Collinge
Author:
S. Mead
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