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Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2

✍ Scribed by Cardani, Rosanna; Giagnacovo, Marzia; Botta, Annalisa; Rinaldi, Fabrizio; Morgante, Alessandra; Udd, Bjarne; Raheem, Olayinka; Penttilä, Sini; Suominen, Tiina; Renna, Laura V.; Sansone, Valeria; Bugiardini, Enrico; Novelli, Giuseppe; Meola, Giovanni


Book ID
118784340
Publisher
Springer
Year
2012
Tongue
English
Weight
592 KB
Volume
259
Category
Article
ISSN
0340-5354

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