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Adult pompe disease with late onset cardiomyopathy

Authors :
Mitrović, Z
Muačević-Katanec, D
Fumić, K
Žarković, K
Merkler, M
Merćep, I
Kisić H
Reiner, Ž
Publication Year :
2009

Abstract

Pompse disease or acid maltase deficiency or glycogenosis type II is rare lysosomal storage disease due to the mutations of acid alpha-glucoside gene (GAA) on chromosome 17q25.

Subjects

Subjects :
pompe disease

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.57a035e5b1ae..8fc9ae6a71cd34fe3e7f6d20e62fb39a

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Authors Abstract Subjects Details