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S Debiais, C Hommet, I Bonnaud, MA Barthez, S Rimbaux, F Riant and A Autret The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literature Cephalalgia 29

Version of Record online: 28 APR 2009 | DOI: 10.1111/j.1468-2982.2009.01884.x

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