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Glycogen storage disease type II (GSD-II), also called Pompe disease, and formerly known as GSD-IIa or Limbgirdle muscular dystrophy 2V, is an autosomal recessive metabolic disorder 1 which damages muscle and nerve cells throughout the body. It is caused by an accumulation of glycogen in the lysosome due to a deficiency of the lysosomal acid alpha-glucosidase enzyme (GAA). The inability ... This aspect of Pompes Funbres Et Marbrerie Zimmermann Saint Di Des Vosges plays a vital role in practical applications.
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Moreover, pompes disease, hereditary defect in the bodys ability to metabolize glycogen, resulting in a muscle disorder that is usually fatal during the first year of life. The defect responsible, absence of the enzyme alpha-1,4-glucosidase, is extremely rare, occurring in fewer than one in every 150,000. This aspect of Pompes Funbres Et Marbrerie Zimmermann Saint Di Des Vosges plays a vital role in practical applications.
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Glycogen storage disease type II (GSD-II), also called Pompe disease, and formerly known as GSD-IIa or Limbgirdle muscular dystrophy 2V, is an autosomal recessive metabolic disorder 1 which damages muscle and nerve cells throughout the body. It is caused by an accumulation of glycogen in the lysosome due to a deficiency of the lysosomal acid alpha-glucosidase enzyme (GAA). The inability ... This aspect of Pompes Funbres Et Marbrerie Zimmermann Saint Di Des Vosges plays a vital role in practical applications.
Furthermore, pompes disease - Encyclopedia Britannica. This aspect of Pompes Funbres Et Marbrerie Zimmermann Saint Di Des Vosges plays a vital role in practical applications.
Moreover, this dictionary definitions page includes all the possible meanings, example usage and translations of the word Pompes. Did you actually mean pampas or pompous? This aspect of Pompes Funbres Et Marbrerie Zimmermann Saint Di Des Vosges plays a vital role in practical applications.
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- Glycogen storage disease type II - Wikipedia.
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Throughout this comprehensive guide, we've explored the essential aspects of Pompes Funbres Et Marbrerie Zimmermann Saint Di Des Vosges. Pompes disease, hereditary defect in the bodys ability to metabolize glycogen, resulting in a muscle disorder that is usually fatal during the first year of life. The defect responsible, absence of the enzyme alpha-1,4-glucosidase, is extremely rare, occurring in fewer than one in every 150,000. By understanding these key concepts, you're now better equipped to leverage pompes funbres et marbrerie zimmermann saint di des vosges effectively.
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