CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine-Reference-Cited by-同舟云学术

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine

Published:2008-04-09 Issue:5 Volume:74 Page:481-485
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Stam AH,Vanmolkot KRJ,Kremer HPH,Gärtner J,Brown J,Leshinsky-Silver E,Gilad R,Kors EE,Frankhuizen WS,Ginjaar HB,Haan J,Frants RR,Ferrari MD,Van Den Maagdenberg AMJM,Terwindt GM

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.00996.x/fullpdf

Reference19 articles.

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2. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine;Dichgans;Lancet,2005

3. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2;De Fusco;Nat Genet,2003

4. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4;Ophoff;Cell,1996

5. The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief no. 957 Online;Vanmolkot;Hum Mutat,2007

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