Genotype-phenotype correlation in Pompe disease, a step forward

BACKGROUND: Pompe’s disease is a progressive myopathy caused by mutations in the lysosomal enzyme acid alphaglucosidase gene (GAA). A wide clinical variability occurs also in patients sharing the same GAA mutations, even within the same family. METHODS: For a large series of GSDII patients we collec...

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Detalles Bibliográficos
Autores principales: De Filippi, Paola, Saeidi, Kolsoum, Ravaglia, Sabrina, Dardis, Andrea, Angelini, Corrado, Mongini, Tiziana, Morandi, Lucia, Moggio, Maurizio, Di Muzio, Antonio, Filosto, Massimiliano, Bembi, Bruno, Giannini, Fabio, Marrosu, Giovanni, Rigoldi, Miriam, Tonin, Paola, Servidei, Serenella, Siciliano, Gabriele, Carlucci, Annalisa, Scotti, Claudia, Comelli, Mario, Toscano, Antonio, Danesino, Cesare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4249737/
https://www.ncbi.nlm.nih.gov/pubmed/25103075
http://dx.doi.org/10.1186/s13023-014-0102-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4249737/
https://www.ncbi.nlm.nih.gov/pubmed/25103075
http://dx.doi.org/10.1186/s13023-014-0102-z

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