TY  - GEN
AU  - Jurkat-Rott,K
AU  - Freilinger,T
AU  - Dreier,J P
AU  - Herzog,J
AU  - Göbel,H
AU  - Petzold,G C
AU  - Montagna,P
AU  - Gasser,T
AU  - Lehmann-Horn,F
AU  - Dichgans,M
TI  - Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
SN  - 1526-632X
PY  - 2004///1026
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Amino Acid Sequence
KW  - Amino Acid Substitution
KW  - Coma
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Epilepsy
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Genotype
KW  - Hemiplegia
KW  - enzymology
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Middle Aged
KW  - Migraine Disorders
KW  - Models, Molecular
KW  - Molecular Sequence Data
KW  - Mutation, Missense
KW  - Penetrance
KW  - Phenotype
KW  - Point Mutation
KW  - Recurrence
KW  - Sequence Alignment
KW  - Sequence Homology, Amino Acid
KW  - Sodium-Potassium-Exchanging ATPase
KW  - chemistry
N1  - Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/01.wnl.0000127310.11526.fd
ER  -