Familial Ebstein’s anomaly: whole exome sequencing identifies novel phenotype associate with FLNA
Familial Ebstein’s anomaly: whole exome sequencing identifies novel phenotype associate with FLNA
Mercer, Catherine
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Andreoletti, Gaia
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Carroll, Aisling
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Salmon, Anthony P.
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Temple, I. Karen
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Ennis, Sarah
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Mercer, Catherine
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Andreoletti, Gaia
75cfc74e-f938-48c8-b3d5-5b377297d008
Carroll, Aisling
19fefd8d-b71f-4a62-8e4a-aedf75903750
Salmon, Anthony P.
fef1b05b-8bb8-45ab-8183-73f422c1955c
Temple, I. Karen
d63e7c66-9fb0-46c8-855d-ee2607e6c226
Ennis, Sarah
7b57f188-9d91-4beb-b217-09856146f1e9
Mercer, Catherine, Andreoletti, Gaia, Carroll, Aisling, Salmon, Anthony P., Temple, I. Karen and Ennis, Sarah
(2017)
Familial Ebstein’s anomaly: whole exome sequencing identifies novel phenotype associate with FLNA.
Circulation: Cardiovascular Genetics, 10 (6).
(doi:10.1161/circgenetics.116.001683).
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Circulation Cardiovascular Genetics 6th Sept 2017 manuscript cleaned
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Clinical Perspective 1 Sept 2017
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Accepted/In Press date: 20 September 2017
e-pub ahead of print date: 13 December 2017
Identifiers
Local EPrints ID: 414255
URI: http://eprints.soton.ac.uk/id/eprint/414255
ISSN: 1942-325X
PURE UUID: 36d9ce99-78c7-480c-ae08-334c61bce1d9
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Date deposited: 21 Sep 2017 16:31
Last modified: 16 Mar 2024 05:45
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Contributors
Author:
Catherine Mercer
Author:
Gaia Andreoletti
Author:
Aisling Carroll
Author:
Anthony P. Salmon
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