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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
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
0006-8950
706-720
Beck, J.
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Rohrer, J.D.
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Campbell, T.
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Isaacs, A.
dad7b908-f71a-45a0-9f6c-782e2c05d1ea
Morrison, K.E.
f00890f0-2fde-4dbd-a73b-7422e1b0ede8
Goodall, E.F.
fab15975-65f1-4a33-a282-4e85bad0733d
Warrington, E.K.
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Stevens, J.
29a165ee-3c6f-49cc-a261-9769be893dbb
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.
b4e98969-79ee-49c9-9357-06979d5e88ff
Mead, S.
f65de049-47a8-479b-ae10-5d5a73bc27e7
Beck, J.
8246ed92-e608-420b-ad57-7a0fdcfe0b9d
Rohrer, J.D.
7ee3ae42-4689-4887-aadf-c353a3163c2b
Campbell, T.
33dfe406-da80-4386-b7f9-cd1724025000
Isaacs, A.
dad7b908-f71a-45a0-9f6c-782e2c05d1ea
Morrison, K.E.
f00890f0-2fde-4dbd-a73b-7422e1b0ede8
Goodall, E.F.
fab15975-65f1-4a33-a282-4e85bad0733d
Warrington, E.K.
2430c2e2-b1a0-4ce1-af68-6477fb2ed0ff
Stevens, J.
29a165ee-3c6f-49cc-a261-9769be893dbb
Revesz, T.
e5a3813b-4e1b-4846-a51f-838427820661
Holton, J.
a26855b2-89dc-492f-a238-ca737514aa93
Al-Sarraj, S.
fe4cc343-909a-4297-b70c-3da9f0e573dd
King, A.
460f716f-e5d7-4962-83a8-6c5c04bd067a
Scahill, R.
561486a4-801a-4720-9132-b550773bcf6d
Warren, J.D.
a3dabb66-ceec-4895-babc-8dd8d2f3a79c
Fox, N.C.
16f9c9fe-56c7-4ffa-b7cd-6095aba4ecfc
Rossor, M.N.
2818d9e6-326f-467b-805f-8e5ddd908af2
Collinge, J.
b4e98969-79ee-49c9-9357-06979d5e88ff
Mead, S.
f65de049-47a8-479b-ae10-5d5a73bc27e7

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), 706-720. (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: https://eprints.soton.ac.uk/id/eprint/398777
ISSN: 0006-8950
PURE UUID: f407230c-221c-4c80-9d37-03b662bc9513
ORCID for K.E. Morrison: ORCID iD orcid.org/0000-0003-0216-5717

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Date deposited: 02 Aug 2016 10:27
Last modified: 06 Jun 2018 12:19

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Contributors

Author: J. Beck
Author: J.D. Rohrer
Author: T. Campbell
Author: A. Isaacs
Author: K.E. Morrison ORCID iD
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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