(Q33674118)

28 July 2017

Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate (English)

1 reference

28 July 2017

0 references

Holmgren G

1

1 reference

28 July 2017

Costa PM

2

1 reference

28 July 2017

Andersson C

3

1 reference

28 July 2017

Asplund K

4

1 reference

28 July 2017

Steen L

5

1 reference

28 July 2017

Beckman L

6

1 reference

28 July 2017

Nylander PO

7

1 reference

28 July 2017

Teixeira A

8

1 reference

28 July 2017

Saraiva MJ

9

1 reference

28 July 2017

Costa PP

10

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 May 1994

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

31

1 reference

28 July 2017

351-354

1 reference

28 July 2017

5

1 reference

Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049863

Linkage of G8 (D4S10) in two Swedish families with Huntington's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049863

Population studies in northern Sweden. XVII. Estimates of Finnish and Saamish influence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049863

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049863

Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049863

Polymorphism of human plasma thyroxine binding prealbumin.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049863

Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049863

X-ray diffraction studies on amyloid filaments

30 October 2018

1 reference

12 December 2020

Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy

1 reference

12 December 2020

Structurally abnormal transthyretin causing familial amyloidotic polyneuropathy in Sweden

1 reference

12 December 2020

Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy

1 reference

12 December 2020

Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences

1 reference

12 December 2020

Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy

1 reference

12 December 2020

Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences

1 reference

12 December 2020

Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy

1 reference

12 December 2020

Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy

1 reference

12 December 2020

Immunoassay for transthyretin variants associated with amyloid neuropathy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.31.5.351

1 reference

28 July 2017

1 reference

28 July 2017

1 reference