A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers

• Main Authors: Olsson Malin (Author), Norgren Nina (Author), Obayashi Konen (Author), Plante-Bordeneuve Violaine (Author), Suhr Ole B (Author), Cederquist Kristina (Author), Jonasson Jenni (Author)
• Format: Book
• Published: BMC, 2010-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<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...