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Autor:
Kun-Ze eLee, Kai eQiu, Milapjit S Sandhu, Mai K Elmallah, Darin J Falk, Michael A Lane, Paul J Reier, Barry J Byrne, David D Fuller
Publikováno v:
Frontiers in Physiology, Vol 2 (2011)
Pompe disease is a lysosomal storage disorder associated with systemic deficiency of acid α-glucosidase (GAA). Respiratory-related problems in Pompe disease include hypoventilation and upper airway dysfunction. Although these problems have genera
Externí odkaz:
https://doaj.org/article/d69dc30c5aaa436aa94abbd1985dd7d9
