Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

2001 ◽  
Vol 7 (3) ◽  
pp. 249-256 ◽  
Author(s):  
Petra M. Jakobs ◽  
Emily L. Hanson ◽  
Kathy A. Crispell ◽  
Warren Toy ◽  
Hugh Keegan ◽  
...  
Author(s):  
Drissa Mariem ◽  
◽  
Yaakoubi Wael ◽  
Helali Sana ◽  
Hbiba Drissa ◽  
...  

Mutation in LMNA accounts for 10% of Dilated Cardiomyopathy (DCM). It is characterised by progressive conduction system disease, arrhythmia and systolic impairment, lamin A/C heart disease is the most malignant gene common in DCMs especially in man. It is likely to be an under-recognised cause of this cardiomyopathy. In certain clinical scenarios, particularly familial DCM with early conduction disease, the probability of finding an LMNA mutation may be quite high.


1999 ◽  
Vol 341 (23) ◽  
pp. 1715-1724 ◽  
Author(s):  
Diane Fatkin ◽  
Calum MacRae ◽  
Takeshi Sasaki ◽  
Matthew R. Wolff ◽  
Maurizio Porcu ◽  
...  

2008 ◽  
Vol 44 (2) ◽  
pp. 293-303 ◽  
Author(s):  
Cordula M. Wolf ◽  
Libin Wang ◽  
Ronny Alcalai ◽  
Anne Pizard ◽  
Patrick G. Burgon ◽  
...  

2016 ◽  
Vol 4 (3) ◽  
pp. 232470961665849
Author(s):  
Ragesh Panikkath ◽  
Deepa Panikkath ◽  
S. Sanchez-Iglesias ◽  
D Araujo-Vilar ◽  
Joaquin Lado-Abeal

1994 ◽  
Vol 7 (4) ◽  
pp. 546-551 ◽  
Author(s):  
Susan Kass ◽  
Calum MacRae ◽  
Harry L. Graber ◽  
Elizabeth A. Sparks ◽  
Dennis McNamara ◽  
...  

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