Condition: Migraine, Familial Hemiplegic, 3
rs121918632 in
LOC102724058;SCN1A-AS1;SCN1A gene and
Migraine, Familial Hemiplegic, 3
PMID 19332696 2009 Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
PMID 17397047 2007 The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
PMID 16054936 2005 Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
PMID 18021921 2007 Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
rs121918628 in
SCN1A-AS1;LOC102724058;SCN1A gene and
Migraine, Familial Hemiplegic, 3
PMID 17397047 2007 The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
PMID 16054936 2005 Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
PMID 18021921 2007 Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
PMID 19332696 2009 Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
rs121918799 in
SCN1A-AS1;SCN1A;LOC102724058 gene and
Migraine, Familial Hemiplegic, 3
PMID 16054936 2005 Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
PMID 19332696 2009 Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
PMID 17397047 2007 The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
PMID 18021921 2007 Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.