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Prevalence of Acid alpha-Glucosidase (GAA) Pseudodefiency Allele and It’s Clinical Significance Among Patients with Cardiomyopathy

Background: Pompe disease is an autosomal recessive lysosomal storage disorder caused by deficiency of lysosomal acid alpha-glucosidase (GAA) activity, leading to the progressive accumulation of glycogen in lysosomes of the skeletal and cardiac muscles. An alpha-glucosidase (GAA) pseudodeficiency a...

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Main Authors: Han Bing, Chow, H, S,, Ling, E. Z., Chan, B. K., Chung, L. K.`, Then, I. X., Pang, H. K., Khor, S. T., Chan, C. T., Tan, K. T.`, Koh, Y. L., Cham, Asri, Said, A. Y. Y., Fong, T. K., Ong, Y. Y., Oon
Format: Article
Language:English
Published: Elsevier B.V. 2022
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R Medicine (General)
Online Access:http://ir.unimas.my/id/eprint/41001/3/Prevalence.pdf
http://ir.unimas.my/id/eprint/41001/
https://www.clinicalkey.com/#!/content/playContent/1-s2.0-S0167527322015492?returnurl=https:%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0167527322015492%3Fshowall%3Dtrue&referrer=https:%2F%2Fwww.internationaljournalofcardiology.com%2F
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http://ir.unimas.my/id/eprint/41001/
https://www.clinicalkey.com/#!/content/playContent/1-s2.0-S0167527322015492?returnurl=https:%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0167527322015492%3Fshowall%3Dtrue&referrer=https:%2F%2Fwww.internationaljournalofcardiology.com%2F

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