A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
<p>Abstract</p> <p>Background</p> <p>Familial amyloidosis with polyneuropathy (FAP) is an autosomal dominant disease caused by transthyretin (<it>TTR</it>) mutations, of which V30M (<it>TTR </it>c.148G > A, p.Val50Met, "Val30Met") is...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2010-09-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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