Cardiomyopathy in congenital complete lipodystrophy
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.610407.x/fullpdf
Reference30 articles.
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2. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy;Bonne;Nat Genet,1999
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. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B);Muchir;Hum Mol Genet,2000
5. The envelope, please: nuclear lamins and disease;Hegele;Nat Med,2000
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