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Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation)

PaperCitations, authors & open-access status

Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) is a paper indexed in PICO Portal from OpenAlex.

How many citations does Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) have?

PICO Portalcitation count

Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) has 54 citations in the OpenAlex counts PICO Portal stores.

When was Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) published?

PICO Portalyear

Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) has 2018 year in the PICO Portal index.

What is the open-access status of Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation)?

PICO Portaloa status

Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) has closed oa status in the PICO Portal index.

What is the DOI of Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation)?

PICO Portaldoi

The DOI for Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) is on the source record.

What is the PMID of Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation)?

PICO Portalpmid

The PMID for Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) is on the source record.

What is the OpenAlex record for Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation)?

PICO Portalopenalex

The OpenAlex for Angiographic Signatures of the Predominant Form of Familial Transthyretin Amyloidosis (Val30Met Mutation) is on the source record.

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