Glycogen storage disease type II (also called Pompe disease / ˈ p ɒ m p ə / or acid maltase deficiency) is an autosomal recessive metabolic disorder  which ...
Glycogen storage disease type II (GSD II), or Pompe disease, is classified by age of onset, organ involvement, severity, and rate of progression.
Glycogen-storage disease type II (GSDII), also referred to as Pompe disease, is an autosomal recessive disorder that results from the deficiency of acid ...
Glycogen storage disease type 2, also known as Pompe disease or acid maltase deficiency disease, is an inherited metabolic disorder caused by an inborn ...
Glycogen storage disease type II | definition of Glycogen storage disease type II by Medical dictionary
Glycogen storage disease type III (also known as GSDIII or Cori disease) is an inherited disorder caused by the buildup of a complex sugar called ...
Glycogen storage disease II, an autosomal recessive disorder, ... Glycogen storage disease type II is inherited as an autosomal recessive trait. Smith et al. ...
Pompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the ... Glycogen Storage Disease Type II (Pompe Disease)
Glycogen storage disease type II. Glycogen storage disease type II (also called Pompe disease or infantile acid maltase deficiency) is a rare genetic disorder caused ...
Glycogen storage disease type II (Pompe's Disease) is a disease that causes glycogen to accumulate in lysosomes