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Ryanodine Receptor Mutations Presenting as Idiopathic Ventricular Fibrillation: A Report on Two Novel Familial Compound Mutations, c.6224T>C and c.13781A>G, With the Clinical Presentation of Idiopathic Ventricular Fibrillation

✍ Scribed by Paech, Christian; Gebauer, Roman Antonin; Karstedt, Jens; Marschall, Christoph; Bollmann, Andreas; Husser, Daniela


Book ID
124159200
Publisher
Springer
Year
2014
Tongue
English
Weight
199 KB
Volume
35
Category
Article
ISSN
0172-0643

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