Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation

Una Marie Sheerin; Maria Stamelou; Gavin Charlesworth; Tamara Shiner; Sian Spacey; Enza Maria Valente; Nicholas W. Wood; Kailash P. Bhatia

doi:10.1007/s00415-012-6747-4

Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation

Una Marie Sheerin, Maria Stamelou, Gavin Charlesworth, Tamara Shiner, Sian Spacey, Enza Maria Valente, Nicholas W. Wood, Kailash P. Bhatia^*

^*Corresponding author for this work

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

15 Scopus citations

Original language	English
Pages (from-to)	656-660
Number of pages	5
Journal	Journal of Neurology
Volume	260
Issue number	2
DOIs	https://doi.org/10.1007/s00415-012-6747-4
State	Published - Feb 2013
Externally published	Yes

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10.1007/s00415-012-6747-4

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title = "Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation",

author = "Sheerin, {Una Marie} and Maria Stamelou and Gavin Charlesworth and Tamara Shiner and Sian Spacey and Valente, {Enza Maria} and Wood, {Nicholas W.} and Bhatia, {Kailash P.}",

note = "Funding Information: This study was supported by the Medical Research Council and Wellcome Trust disease centre (grant WT089698/Z/09/Z). DNA extraction work was undertaken at University College London Hospitals, University College London, who received a proportion of funding from the Department of Health{\textquoteright}s National Institute for Health Research Biomedical Research Centres funding. ",

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AU - Sheerin, Una Marie

AU - Stamelou, Maria

AU - Charlesworth, Gavin

AU - Shiner, Tamara

AU - Spacey, Sian

AU - Valente, Enza Maria

AU - Wood, Nicholas W.

AU - Bhatia, Kailash P.

N1 - Funding Information: This study was supported by the Medical Research Council and Wellcome Trust disease centre (grant WT089698/Z/09/Z). DNA extraction work was undertaken at University College London Hospitals, University College London, who received a proportion of funding from the Department of Health’s National Institute for Health Research Biomedical Research Centres funding.

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Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation

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