Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration. [electronic resource]
Producer: 20070105Description: 829-43 p. digitalISSN:- 0300-9564
- Aged
- Auditory Diseases, Central -- genetics
- Brain Stem -- pathology
- Cerebellum -- pathology
- DNA Mutational Analysis
- Deglutition Disorders -- genetics
- Female
- Genotype
- Germany
- Humans
- Immunohistochemistry
- Male
- Middle Aged
- Mutation -- genetics
- Nerve Degeneration -- pathology
- Neurons -- pathology
- Ocular Motility Disorders -- genetics
- Pedigree
- Peptides -- genetics
- Sensation Disorders -- genetics
- Spinocerebellar Ataxias -- genetics
- Trinucleotide Repeat Expansion -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.