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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Materyal Türü: | Kitap |
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BMC,
2003-07-01T00:00:00Z.
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Yer Numarası: |
A1234.567 |
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Kopya Bilgisi 1 | Kütüphanede |