Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients. [electronic resource]
Producer: 20000413Description: 205-11 p. digitalISSN:- 1364-6745
- Adult
- Age of Onset
- Alleles
- Alternative Splicing
- Amino Acid Sequence
- Amino Acid Substitution
- Base Sequence
- DNA -- chemistry
- DNA Mutational Analysis
- Genetic Heterogeneity
- Germany
- Glycogen Storage Disease Type II -- enzymology
- Humans
- Introns -- genetics
- Lysosomes -- enzymology
- Middle Aged
- Mutagenesis, Insertional
- Phenotype
- Point Mutation
- Sequence Deletion
- Sequence Homology, Amino Acid
- Sequence Homology, Nucleic Acid
- alpha-Glucosidases -- deficiency
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.