TY  - GEN
AU  - Kaunisto,M A
AU  - Harno,H
AU  - Vanmolkot,K R J
AU  - Gargus,J J
AU  - Sun,G
AU  - Hämäläinen,E
AU  - Liukkonen,E
AU  - Kallela,M
AU  - van den Maagdenberg,A M J M
AU  - Frants,R R
AU  - Färkkilä,M
AU  - Palotie,A
AU  - Wessman,M
TI  - A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
SN  - 1364-6745
PY  - 2004///0924
KW  - Amino Acid Sequence
KW  - Chromosomes, Human, Pair 1
KW  - Family Health
KW  - Female
KW  - Finland
KW  - Gene Frequency
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Hemiplegia
KW  - genetics
KW  - Humans
KW  - Male
KW  - Migraine Disorders
KW  - Molecular Sequence Data
KW  - Mutation, Missense
KW  - Pedigree
KW  - Sodium-Potassium-Exchanging ATPase
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1007/s10048-004-0178-z
ER  -