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Galactosialidosis: review and analysis of CTSA gene mutations

BACKGROUND: Mutations in the CTSA gene, that encodes the protective protein/cathepsin A or PPCA, lead to the secondary deficiency of β-galactosidase (GLB1) and neuraminidase 1 (NEU1), causing the lysosomal storage disorder galactosialidosis (GS). Few clinical cases of GS have been reported in the li...

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Detalles Bibliográficos
Autores principales:	Caciotti, Anna, Catarzi, Serena, Tonin, Rodolfo, Lugli, Licia, Perez, Carmen Rodriguez, Michelakakis, Helen, Mavridou, Irene, Donati, Maria Alice, Guerrini, Renzo, d’Azzo, Alessandra, Morrone, Amelia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737020/ https://www.ncbi.nlm.nih.gov/pubmed/23915561 http://dx.doi.org/10.1186/1750-1172-8-114

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