Genetic Heterogeneity of Familial Hemiplegic Migraine

Familial hemiplegic migraine (FHM) is an autosomal dominant variety of migraine with aura. We previously mapped a gene responsible for this disorder to the short arm of chromosome 19, within a 30-cM interval bracketed by D19S216 and D19S215. Linkage analysis conducted on two large pedigrees did not...

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Bibliografische gegevens
Hoofdauteurs: Joutel, A., Ducros, A., Vahedi, K., Labauge, P., Delrieu, O., Pinsard, N., Mancini, J., Ponsot, G., Gouttière, F., Gastaut, J. L., Maziaceck, J., Weissenbach, J., Bousser, M. G., Tournier-Lasserve, E.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1994
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Original Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918426/
https://ncbi.nlm.nih.gov/pubmed/7977376
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