Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Tabulation of transthyretin (TTR) variants as of 1/1/2000.

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis - 1 Mar 2000

Connors L H, Richardson A M, Théberge R, Costello C E

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alzheimer's disease research and treatments
Share to Amino Acid Sequence
Share to Amyloidosis: Diagnosis, Treatment, Outcomes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Databases, Factual

Share to TTR gene

Share to Molecular Sequence Data

Share to Mutation

Share to Prealbumin

Source

Identifiers

PMID: 10842707
DOI: 10.3109/13506120009146826

Genes

TTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Tabulation of transthyretin (TTR) variants as of 1/1/2000.PMID 10842707Read ↗

Tabulation of human transthyretin (TTR) variants, 2003.Semantic proximity Read ↗

Follow-up regimens for carriers of hereditary transthyretin variants.Semantic proximity Read ↗

[Non-autoimmune hyperthyroidism].Semantic proximity Read ↗

The role of transthyretin in cell biology: impact on human pathophysiologySemantic proximity Read ↗

Genetic phenotypes and clinical characteristics description of hereditary transthyretin patients in ChinaSemantic proximity Read ↗

[Recommendations update for the diagnosis and treatment of transthyretin variant amyloidosis (ATTRv)].Semantic proximity Read ↗

Inherited defects of thyroxine-binding proteins.Semantic proximity Read ↗

[Immunological and serological laboratory tests: transthyretin].Semantic proximity Read ↗

[Thyroglobulin gene abnormalities].Semantic proximity Read ↗

[Thyroglobulin gene abnormalities].Semantic proximity Read ↗

Congenital thyrotropin deficiency--from discovery to molecular biology, postgenome and preventive medicine.Semantic proximity Read ↗

Hereditary transthyretin amyloidosisSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.