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HAPLOTYPE ANALYSIS OF COMMON TRANSTHYRETIN MUTATIONS

Title
HAPLOTYPE ANALYSIS OF COMMON TRANSTHYRETIN MUTATIONS
Type
Another Publication in an International Scientific Journal
Year
1995
Authors
ALMEIDA, MR
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AOYAMAOISHI, N
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SAKAKI, Y
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HOLMGREN, G
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ULF, D
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FERLINI, A
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SALVI, F
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MUNARQUES, M
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BENSON, MD
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SKINNER, M
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COSTA, PP
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SARAIVA, MJ
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ICBAS
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Journal
Title: Human GeneticsImported from Authenticus Search for Journal Publications
Vol. 96
Pages: 350-354
ISSN: 0340-6717
Publisher: Springer Nature
Scientific classification
FOS: Natural sciences > Earth and related Environmental sciences
Other information
Authenticus ID: P-001-GCW
Abstract (EN): The most frequent transthyretin (TTR) variant associated with hereditary amyloidosis is TTR Met 30, which has its major focus in Portugal, although it also occurs in many other countries, The distribution of the mutation and its occurrence in a CpG dinucleotide lead us to question the origin of the mutation and the possibility of its having originated in Portugal. In order to investigate these questions, we studied the distribution of haplotypes associated with the Met 30 mutation in families from different European countries. All the analysed Portuguese families presented the same haplotype associated with the Met 30 mutation (haplotype I). The same was found for the Swedish and Spanish families studied, However, a distinct haplotype (haplotype III) was found in three families, one Italian, one English and one Turkish. These results suggest that, although the Portuguese Met 30 carriers might have one founder, the mutation probably recurred in populations in Europe in a similar manner to that reported in Japan. In this study, we have also analysed the haplotypes associated with other TTR variants frequent in the Portuguese population.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 5
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