Identification of variants in the acid α-glucosidase (GAA) gene in Pompe disease provides valuable insights and systematic overviews are needed. We report on the number, nature, frequency, and geographic distribution of GAA sequence variants listed in the Pompe Regis
PurposeTo characterize clinical characteristics and genotypes of patients in the ADVANCE study of 40...
Objective To report the clinical features and acid alpha-glucosidase(GAA) gene mutations of Chinese ...
Pompe disease is an autosomal recessive disorder linked to GAA gene that leads to a multi-system int...
Identification of variants in the acid α-glucosidase (GAA) gene in Pompe disease provides valuable i...
Identification of variants in the acid α-glucosidase (GAA) gene in Pompe disease provides valuable i...
Pompe disease is an inherited disorder caused by disease-associated variants in the acid α-glucosida...
Pompe disease is a metabolic disorder caused by a deficiency of the glycogen-hydrolyzing lysosomal e...
Pompe disease is an autosomal recessive lysosomal storage disorder caused by disease‐associated var...
The main subject addressed in this thesis is the genotype-phenotype relationship in Pompe disease. P...
[Background] Pompe disease (PD) is an autosomal recessive metabolic disorder caused by pathogenic va...
Background: Pompe disease (Glycogen storage disease type II, GSD II, acid alpha-glucosidase deficien...
Pompe disease (PD) is an autosomal recessive metabolic disorder caused by pathogenic variants in the...
Pompe disease, or glycogen storage disease II is a rare, progressive disease leading to skeletal mus...
textabstractBackground: Pompe disease (Glycogen storage disease type II, GSD II, acid alpha-glucosid...
Background: Pompe's disease is a progressive myopathy caused by mutations in the lysosomal enzyme ac...
PurposeTo characterize clinical characteristics and genotypes of patients in the ADVANCE study of 40...
Objective To report the clinical features and acid alpha-glucosidase(GAA) gene mutations of Chinese ...
Pompe disease is an autosomal recessive disorder linked to GAA gene that leads to a multi-system int...
Identification of variants in the acid α-glucosidase (GAA) gene in Pompe disease provides valuable i...
Identification of variants in the acid α-glucosidase (GAA) gene in Pompe disease provides valuable i...
Pompe disease is an inherited disorder caused by disease-associated variants in the acid α-glucosida...
Pompe disease is a metabolic disorder caused by a deficiency of the glycogen-hydrolyzing lysosomal e...
Pompe disease is an autosomal recessive lysosomal storage disorder caused by disease‐associated var...
The main subject addressed in this thesis is the genotype-phenotype relationship in Pompe disease. P...
[Background] Pompe disease (PD) is an autosomal recessive metabolic disorder caused by pathogenic va...
Background: Pompe disease (Glycogen storage disease type II, GSD II, acid alpha-glucosidase deficien...
Pompe disease (PD) is an autosomal recessive metabolic disorder caused by pathogenic variants in the...
Pompe disease, or glycogen storage disease II is a rare, progressive disease leading to skeletal mus...
textabstractBackground: Pompe disease (Glycogen storage disease type II, GSD II, acid alpha-glucosid...
Background: Pompe's disease is a progressive myopathy caused by mutations in the lysosomal enzyme ac...
PurposeTo characterize clinical characteristics and genotypes of patients in the ADVANCE study of 40...
Objective To report the clinical features and acid alpha-glucosidase(GAA) gene mutations of Chinese ...
Pompe disease is an autosomal recessive disorder linked to GAA gene that leads to a multi-system int...