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Dive into the research topics of 'Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2'. Together they form a unique fingerprint.- Sort by
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Rosanna Cardani, Marzia Giagnacovo, Annalisa Botta, Fabrizio Rinaldi, Alessandra Morgante, Bjarne Udd, Olayinka Raheem, Sini Penttilä, Tiina Suominen, Laura V. Renna, Valeria Sansone, Enrico Bugiardini, Giuseppe Novelli, Giovanni Meola
Research output: Contribution to journal › Article › peer-review