Genotype-phenotype correlation in Pompe disease, a step forward

Paola De Filippi, Paola De Filippi, Paola De Filippi, Kolsoum Saeidi, Kolsoum Saeidi, Kolsoum Saeidi, Sabrina Ravaglia, Sabrina Ravaglia, Sabrina Ravaglia, Andrea Dardis, Andrea Dardis, Andrea Dardis, Corrado Angelini, Corrado Angelini, Corrado Angelini, Tiziana Mongini, Tiziana Mongini, Tiziana Mongini, Lucia Morandi, Lucia Morandi, Lucia Morandi, Maurizio Moggio, Maurizio Moggio, Maurizio Moggio, Antonio Di Muzio, Antonio Di Muzio, Antonio Di Muzio, Massimiliano Filosto, Massimiliano Filosto, Massimiliano Filosto, Bruno Bembi, Bruno Bembi, Bruno Bembi, Fabio Giannini, Fabio Giannini, Fabio Giannini, Giovanni Marrosu, Giovanni Marrosu, Giovanni Marrosu, Miriam Rigoldi, Miriam Rigoldi, Miriam Rigoldi, Paola Tonin, Paola Tonin, Paola Tonin, Serenella Servidei, Serenella Servidei, Serenella Servidei, Gabriele Siciliano, Gabriele Siciliano, Gabriele Siciliano, Annalisa Carlucci, Annalisa Carlucci, Annalisa Carlucci, Claudia Scotti, Claudia Scotti, Claudia Scotti, Mario Comelli, Mario Comelli, Mario Comelli, Antonio Toscano, Antonio Toscano, Antonio Toscano, Cesare Danesino, Cesare Danesino, Cesare Danesino
  • Orphanet Journal of Rare Diseases, August 2014, Springer Science + Business Media
  • DOI: 10.1186/s13023-014-0102-z

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http://dx.doi.org/10.1186/s13023-014-0102-z

The following have contributed to this page: Prof Corrado Angelini