TY  - GEN
AU  - Vorgerd,M
AU  - Burwinkel,B
AU  - Reichmann,H
AU  - Malin,J P
AU  - Kilimann,M W
TI  - Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients
SN  - 1364-6745
PY  - 2000///0413
KW  - Adult
KW  - Age of Onset
KW  - Alleles
KW  - Alternative Splicing
KW  - Amino Acid Sequence
KW  - Amino Acid Substitution
KW  - Base Sequence
KW  - DNA
KW  - chemistry
KW  - DNA Mutational Analysis
KW  - Genetic Heterogeneity
KW  - Germany
KW  - Glycogen Storage Disease Type II
KW  - enzymology
KW  - Humans
KW  - Introns
KW  - genetics
KW  - Lysosomes
KW  - Middle Aged
KW  - Mutagenesis, Insertional
KW  - Phenotype
KW  - Point Mutation
KW  - Sequence Deletion
KW  - Sequence Homology, Amino Acid
KW  - Sequence Homology, Nucleic Acid
KW  - alpha-Glucosidases
KW  - deficiency
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s100480050030
ER  -