A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers-Reference-Cited by-同舟云学术

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

Published:2010-09-14 Issue:1 Volume:11 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Olsson Malin,Norgren Nina,Obayashi Konen,Plante-Bordeneuve Violaine,Suhr Ole B,Cederquist Kristina,Jonasson Jenni

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-11-130.pdf

Reference30 articles.

1. Hammarstrom P, Jiang X, Hurshman AR, Powers ET, Kelly JW: Sequence-dependent denaturation energetics: A major determinant in amyloid disease diversity. Proc Natl Acad Sci USA. 2002, 99 (Suppl 4): 16427-16432. 10.1073/pnas.202495199.

2. Saraiva MJ: Transthyretin mutations in hyperthyroxinemia and amyloid diseases. Hum Mutat. 2001, 17 (6): 493-503. 10.1002/humu.1132.

3. Drugge U, Andersson R, Chizari F, Danielsson M, Holmgren G, Sandgren O, Sousa A: Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis. J Med Genet. 1993, 30 (5): 388-392. 10.1136/jmg.30.5.388.

4. Hellman U, Alarcon F, Lundgren HE, Suhr OB, Bonaiti-Pellie C, Plante-Bordeneuve V: Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population. Amyloid. 2008, 15 (3): 181-186. 10.1080/13506120802193720.

5. Holmgren G, Costa PM, Andersson C, Asplund K, Steen L, Beckman L, Nylander PO, Teixeira A, Saraiva MJ, Costa PP: Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate. J Med Genet. 1994, 31 (5): 351-354. 10.1136/jmg.31.5.351.

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