The new frame for Mucopolysaccharidoses

Abstract Mucopolysaccharidoses (MPS) are genetic, progressive, lysosomal storage disorders affecting virtually all organs and systems. The first MPS were clinically identified about 100 years ago. Nowadays, the enzyme defects and related genes are known for all 11 different enzyme defects. Treatment...

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Principais autores: Rossella Parini (Autor), Andrea Biondi (Autor)
Formato: Livro
Publicado em: BMC, 2018-11-01T00:00:00Z.
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3rd Floor Main Library

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