MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1

Literature (2)

Literature for OMIM 141500: MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1

Xenbase Articles:
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Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects., Müllner C,Broos LA,van den Maagdenberg AM,Striessnig J, J Biol Chem. December 10, 2004; 279(50):1083-351X.
Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A., García Segarra N,Gautschi I,Mittaz-Crettol L,Al-Qusairi L,Van Bemmelen MX,Maeder P,Schild L,Roulet-Perez E,Kallay Zetchi C,Bonafé L, J Neurol Sci. July 15, 2014; 342(1-2):1878-5883.

Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A., García Segarra N,Gautschi I,Mittaz-Crettol L,Al-Qusairi L,Van Bemmelen MX,Maeder P,Schild L,Roulet-Perez E,Kallay Zetchi C,Bonafé L, J Neurol Sci. July 15, 2014; 342(1-2):1878-5883.