Add to ORKGBackground : Gaucher ((go-SHAY )disease is a rare genetic disorder in which a person lacks an enzyme called glucocerebrosidase (GBA).1 Gaucher disease is an autosomal recessive inherited disorder of metabolism where a type of fat (lipid) called glucocerebroside cannot be adequately degraded. Genome. The lack of the GBA causes harmful substances to build up in the lung, liver, spleen, bones, and bone marrow, brain and eyes. These substances prevent cells and organs from working properly.There are three recognized Types of Gaucher disease and each has a wide range of symptoms. Type 1 is the most common, does not affect the nervous system and may appear early in life or adulthood. Many people with Type 1 Gaucher disease have findings ...
Gaucher's disease is a rare lipid storage disorder, affecting one in 40,000-200,000 people and resul...
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
Gaucher's disease - an overview about a sphingolipidosis Abstract. Gaucher's disease is a sphingolip...
Background : Gaucher ((go-SHAY )disease is a rare genetic disorder in which a person lacks an enzym...
Gaucher disease is a rare autosomal recessive genetic disorder. It is caused by the deficiency of ly...
Gaucher disease (GD, ORPHA355) is a rare, autosomal recessive genetic disorder. It is caused by a de...
Gaucher disease (GD, ORPHA355) is a rare, autosomal recessive genetic disorder. It is caused by a de...
Gaucher disease is caused by mutations in the Gba1 gene encoding an acid β-glucocerebrosidase (GBA1)...
Gaucher disease is a lysosomal storage disorder caused by abnormally low glucocerebrosidase enzy-mat...
Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease ...
Gaucher disease is the autosomally recessively inherited deficiency of the lysosomal enzyme glucocer...
Gaucher’s disease is a lysosomal storage disease caused by the lack of beta-glucocerebrosidase enzym...
Objective Gaucher disease (GD) is a rare inborn error of metabolism, classified as a lipid storage d...
Objective Gaucher disease (GD) is a rare inborn error of metabolism, classified as a lipid storage d...
Gaucher’s syndrome is the distinguished prevailing disorder characterized under the lysosomal reposi...
Gaucher's disease is a rare lipid storage disorder, affecting one in 40,000-200,000 people and resul...
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
Gaucher's disease - an overview about a sphingolipidosis Abstract. Gaucher's disease is a sphingolip...
Background : Gaucher ((go-SHAY )disease is a rare genetic disorder in which a person lacks an enzym...
Gaucher disease is a rare autosomal recessive genetic disorder. It is caused by the deficiency of ly...
Gaucher disease (GD, ORPHA355) is a rare, autosomal recessive genetic disorder. It is caused by a de...
Gaucher disease (GD, ORPHA355) is a rare, autosomal recessive genetic disorder. It is caused by a de...
Gaucher disease is caused by mutations in the Gba1 gene encoding an acid β-glucocerebrosidase (GBA1)...
Gaucher disease is a lysosomal storage disorder caused by abnormally low glucocerebrosidase enzy-mat...
Gaucher disease (GD), the most common inherited lysosomal storage disorder, is a multiorgan disease ...
Gaucher disease is the autosomally recessively inherited deficiency of the lysosomal enzyme glucocer...
Gaucher’s disease is a lysosomal storage disease caused by the lack of beta-glucocerebrosidase enzym...
Objective Gaucher disease (GD) is a rare inborn error of metabolism, classified as a lipid storage d...
Objective Gaucher disease (GD) is a rare inborn error of metabolism, classified as a lipid storage d...
Gaucher’s syndrome is the distinguished prevailing disorder characterized under the lysosomal reposi...
Gaucher's disease is a rare lipid storage disorder, affecting one in 40,000-200,000 people and resul...
Aim: Gaucher disease is a rare lysosomal storage disease. Enzyme replacement therapy has proven to b...
Gaucher's disease - an overview about a sphingolipidosis Abstract. Gaucher's disease is a sphingolip...