Identification of a de Novo point mutation resulting in infantile form of Pompe's disease.

Lin, C Y

Identification of a de Novo point mutation resulting in infantile form of Pompe's disease. [electronic resource] - Biochemical and biophysical research communications Aug 1995 - 367 p. digital

Publication Type: Published Erratum

0006-291X

10.1006/bbrc.1995.2139 doi


Amino Acid Sequence
Aspartic Acid
Base Sequence
Codon
Glycogen Storage Disease Type II--genetics
Humans
Infant
Molecular Sequence Data
Point Mutation
alpha-Glucosidases--genetics