| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10954456 | Journal of Molecular and Cellular Cardiology | 2005 | 7 Pages |
Abstract
Conclusions. - Gene mutations in cTnI occur in Australian families with HCM with a prevalence higher than previously reported and may be associated with a clinically more malignant course, reflecting significant disruptions to troponin complex interactions.
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Authors
Alessandra Doolan, Molly Tebo, Jodie Ingles, Lan Nguyen, Tatiana Tsoutsman, Lien Lam, Christine Chiu, Jessica Chung, Robert G. Weintraub, Christopher Semsarian,