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The Journal of Clinical Investigation|December 6, 2000
An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathyD Fatkin, B K McConnell, J O Mudd, et al.
American Journal of Human Genetics|December 31, 2005
Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotypeD B Sparrow, G Chapman, M A Wouters, et al.
Circulation|June 1, 1994
Exclusion of atrial thrombus by transesophageal echocardiography does not preclude embolism after cardioversion of atrial fibrillation. A multicenter studyI W Black, D Fatkin, K B Sagar, et al.
Circulation|April 19, 2000
Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24J Schönberger, H Levy, E Grünig, et al.
The New England Journal of Medicine|December 2, 1999
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system diseaseD Fatkin, C MacRae, T Sasaki, et al.
Molecular and Cellular Biology|March 10, 2001
Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expressionB G Bruneau, Z Z Bao, D Fatkin, et al.
The Journal of Clinical Investigation|November 5, 1999
Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant miceB K McConnell, K A Jones, D Fatkin, et al.
Circulation Research|March 7, 2001
Comparison of two murine models of familial hypertrophic cardiomyopathyB K McConnell, D Fatkin, C Semsarian, et al.
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