The FHM1 Mutation S218L: A Severe Clinical Phenotype? A Case Report and Review of the Literature

Title
The FHM1 Mutation S218L: A Severe Clinical Phenotype? A Case Report and Review of the Literature
Authors
Keywords
-
Journal
CEPHALALGIA
Volume 29, Issue 12, Pages 1337-1339
Publisher
SAGE Publications
Online
2009-04-28
DOI
10.1111/j.1468-2982.2009.01884.x

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