Novel mutations in PHKA2 gene in glycogen storage disease type IX patients from Hong Kong, China.
Mol Genet Metab
; 102(2): 222-5, 2011 Feb.
Article
in En
| MEDLINE
| ID: mdl-21131218
The diagnosis of glycogen storage disease (GSD) type IX is often complicated by the complexity of the phosphorylase kinase enzyme (PHK), and molecular analysis is the preferred way to provide definitive diagnosis. Here we reported two novel mutations found in two GSD type IX patients with different residual enzyme activities from Hong Kong, China using genetic analysis and, provided the molecular interpretation of the deficient PHK activity. These two newly described mutations would be useful for the study of future GSD patients.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phosphorylase Kinase
/
Glycogen Storage Disease
/
Mutation
Type of study:
Diagnostic_studies
Limits:
Child
/
Child, preschool
/
Humans
/
Male
Country/Region as subject:
Asia
Language:
En
Journal:
Mol Genet Metab
Journal subject:
BIOLOGIA MOLECULAR
/
BIOQUIMICA
/
METABOLISMO
Year:
2011
Document type:
Article
Affiliation country:
China
Country of publication:
United States