Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration.

Bandmann, O

Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration. [electronic resource] - Neurology Dec 1997 - 1598-604 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0028-3878

10.1212/wnl.49.6.1598 doi


Alleles
Animals
Ciliary Neurotrophic Factor
Genotype
Heterozygote
Homozygote
Humans
Insulin-Like Growth Factor I--metabolism
Mice
Mice, Neurologic Mutants--genetics
Multiple System Atrophy--genetics
Mutation
Nerve Tissue Proteins--genetics
Receptors, Somatomedin--genetics
Repetitive Sequences, Nucleic Acid
Sequence Homology, Nucleic Acid
Spinocerebellar Degenerations--genetics