Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy-Reference-Cited by-同舟云学术

Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy

Published:2008-09-15 Issue:1 Volume:104 Page:90-99
ISSN:0300-8428
Container-title:Basic Research in Cardiology
language:en
Short-container-title:Basic Res Cardiol

Author:

Perrot Andreas,Hussein Shwan,Ruppert Volker,Schmidt Hartmut H. J.,Wehnert Manfred S.,Duong Nguyen Thuy,Posch Maximilian G.,Panek Anna,Dietz Rainer,Kindermann Ingrid,Böhm Michael,Michalewska-Wludarczyk Aleksandra,Richter Anette,Maisch Bernhard,Pankuweit Sabine,Özcelik Cemil

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s00395-008-0748-6.pdf

Reference38 articles.

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2. Becker R, Haas M, Ick D, Krueger C, Bauer A, Senges-Becker JC, Voss F, Hilbel T, Niroomand F, Katus HA, Schoels W (2003) Role of nonsustained ventruclar tachycardia and programmed ventricular stimulation for risk stratification in patients with idiopathic dilated cardiomyopathy. Basic Res Cardiol 98:259–266

3. Benedetti S, Menditto I, Degano M, Rodolico C, Merlini L, D’Amico A, Palmucci L, Berardinelli A, Pegoraro E, Trevisan CP, Morandi L, Moroni I, Galluzzi G, Bertini E, Toscano A, Olivè M, Bonne G, Mari F, Caldara R, Fazio R, Mammì I, Carrera P, Toniolo D, Comi G, Quattrini A, Ferrari M, Previtali SC (2007) Phenotypic clustering of lamin A/C mutations in neuromuscular patients. Neurology 69:1285–1292

4. Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F (2000) Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. Ann Neurol 48:170–180

5. Burkett EL, Hershberger RE (2005) Clinical and genetic issues in familial dilated cardiomyopathy. J Am Coll Cardiol 45:969–981

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