TY  - GEN
AU  - Lin,C Y
AU  - Shieh,J J
TI  - Identification of a de Novo point mutation resulting in infantile form of Pompe's disease
SN  - 0006-291X
PY  - 1995///0911
KW  - Amino Acid Sequence
KW  - Aspartic Acid
KW  - Base Sequence
KW  - Codon
KW  - Glycogen Storage Disease Type II
KW  - genetics
KW  - Humans
KW  - Infant
KW  - Molecular Sequence Data
KW  - Point Mutation
KW  - alpha-Glucosidases
N1  - Publication Type: Published Erratum
UR  - https://doi.org/10.1006/bbrc.1995.2139
ER  -