Lamin A/C truncation in dilated cardiomyopathy with conduction disease

<p>Abstract</p> <p>Background</p> <p>Mutations in the gene encoding the nuclear membrane protein lamin A/C have been associated with at least 7 distinct diseases including autosomal dominant dilated cardiomyopathy with conduction system disease, autosomal dominant and r...

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Main Authors: Huber Jill M (Author), Culley Mary R (Author), MacLeod Heather M (Author), McNally Elizabeth M (Author)
Format: Book
Published: BMC, 2003-07-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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