EEG findings in infantile Tay-Sachs disease
β Scribed by Herbert E. Rosenbaum; Joseph M. Stein
- Book ID
- 115859075
- Publisher
- Elsevier Science
- Year
- 1953
- Tongue
- English
- Weight
- 190 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0013-4694
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Two affected HEXA alleles were found in an Israeli Druze Tay-Sachs child born to first-cousin parents. His paternal allele contained two adjacent changes in exon 5: a496C, which resulted in a frameshift and premature termination codon 96 nucleotides downstream, and 498CΓG, a silent mutation. The mat
## Abstract TayβSachs disease and normal fetal cerebellar cells were maintained in culture for up to four weeks. Elevated levels of the lysosomal enzymes hexosaminidase B, Ξ²βgalactosidase, and acid phosphatase were observed in the TayβSachs cells in long term cultures although elevated lysosomal en