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Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_68c41e30acf44131b822b27749f5984e

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

About this item

Full title

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

Publisher

United States: John Wiley & Sons, Inc

Journal title

Annals of clinical and translational neurology, 2023-04, Vol.10 (4), p.553-567

Language

English

Formats

Publication information

Publisher

United States: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Objective
Amyloidosis due to the transthyretin Ser77Tyr mutation (ATTRS77Y) is a rare autosomal‐dominant disorder, characterized by carpal‐tunnel syndrome, poly‐ and autonomic‐neuropathy, and cardiomyopathy. However, related symptoms and signs are often nonspecific and confirmatory tests are required. We describe the age and frequency of early s...

Alternative Titles

Full title

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_68c41e30acf44131b822b27749f5984e

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_68c41e30acf44131b822b27749f5984e

Other Identifiers

ISSN

2328-9503

E-ISSN

2328-9503

DOI

10.1002/acn3.51741

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