A Cardio-Neurological Form of Laminopathy: Dilated Cardiomyopathy with Permanent Partial Atrial Standstill and Axonal Neuropathy
Author:
Publisher
Wiley
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1540-8159.2008.02254.x/fullpdf
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2. Familial dilated cardiomyopathy registry research group. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations;Taylor;J Am Coll Cardiol,2003
3. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease;Fatkin;N Engl J Med,1999
4. Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease;Arbustini;J Am Coll Cardiol,2002
5. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy;Di Barletta;Am J Hum Genet,2000
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