TY  - GEN
AU  - Bandmann,O
AU  - Sweeney,M G
AU  - Daniel,S E
AU  - Wenning,G K
AU  - Quinn,N
AU  - Marsden,C D
AU  - Wood,N W
TI  - Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration
SN  - 0028-3878
PY  - 1998///0116
KW  - Alleles
KW  - Animals
KW  - Ciliary Neurotrophic Factor
KW  - Genotype
KW  - Heterozygote
KW  - Homozygote
KW  - Humans
KW  - Insulin-Like Growth Factor I
KW  - metabolism
KW  - Mice
KW  - Mice, Neurologic Mutants
KW  - genetics
KW  - Multiple System Atrophy
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Receptors, Somatomedin
KW  - Repetitive Sequences, Nucleic Acid
KW  - Sequence Homology, Nucleic Acid
KW  - Spinocerebellar Degenerations
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/wnl.49.6.1598
ER  -