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Expanding the tuberous sclerosis phenotype: mild disease caused by a TSC1 splicing mutation

Expanding the tuberous sclerosis phenotype: mild disease caused by a TSC1 splicing mutation
Expanding the tuberous sclerosis phenotype: mild disease caused by a TSC1 splicing mutation
350-352
Blyth, M.
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Raponi, M.
f465e77f-b9bf-4c32-80d6-43c0787542b9
Treacy, R.
973fc069-4342-4ac1-ac9a-9e2bac0c151d
Raymond, F.L.
c6247c75-486e-4534-b202-7727933c96cd
Yates, J.R.
b252f898-38ab-4496-b6ff-6de31afff6e2
Baralle, D.
faac16e5-7928-4801-9811-8b3a9ea4bb91
Blyth, M.
6d9f76d3-310c-4fda-9890-abcf46c8c62d
Raponi, M.
f465e77f-b9bf-4c32-80d6-43c0787542b9
Treacy, R.
973fc069-4342-4ac1-ac9a-9e2bac0c151d
Raymond, F.L.
c6247c75-486e-4534-b202-7727933c96cd
Yates, J.R.
b252f898-38ab-4496-b6ff-6de31afff6e2
Baralle, D.
faac16e5-7928-4801-9811-8b3a9ea4bb91

Blyth, M., Raponi, M., Treacy, R., Raymond, F.L., Yates, J.R. and Baralle, D. (2010) Expanding the tuberous sclerosis phenotype: mild disease caused by a TSC1 splicing mutation. Journal of Neurology, Neurosurgery, and Psychiatry, 81 (3), 350-352. (doi:10.1136/jnnp.2009.179689).

Record type: Article

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Published date: March 2010

Identifiers

Local EPrints ID: 73116
URI: http://eprints.soton.ac.uk/id/eprint/73116
PURE UUID: cb919016-d082-4c56-bcd3-818c8215aab0
ORCID for D. Baralle: ORCID iD orcid.org/0000-0003-3217-4833

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Date deposited: 02 Mar 2010
Last modified: 26 Nov 2019 01:42

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