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A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?

✍ Scribed by Gutierrez-Roelens, Ilse; Roy, Luc De; Ovaert, Caroline; Sluysmans, Thierry; Devriendt, Koen; Brunner, Han G; Vikkula, Miikka


Book ID
110026703
Publisher
Nature Publishing Group
Year
2006
Tongue
English
Weight
97 KB
Volume
14
Category
Article
ISSN
1018-4813

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