Phenotypes Associated With the Val122Ile, Leu58His, and Late-Onset Val30Met Variants in Patients With Hereditary Transthyretin Amyloidosis-Reference-Cited by-同舟云学术

Phenotypes Associated With the Val122Ile, Leu58His, and Late-Onset Val30Met Variants in Patients With Hereditary Transthyretin Amyloidosis

Published:2023-05-09 Issue:19 Volume:100 Page:
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Zampino Serena¹,Sheikh Farooq H.¹,Vaishnav Joban¹^ORCID,Judge Daniel¹,Pan Baohan¹,Daniel Amrita¹,Brown Emily¹,Ebenezer Gigi¹^ORCID,Polydefkis Michael¹^ORCID

Affiliation:

1. From the Department of Neurology (S.Z., B.P., A.D., G.E., M.P.), Johns Hopkins University School of Medicine, Baltimore, MD; Cardiology (F.H.S.), MedStar Medical Group, Washington, DC; Division of Cardiology (J.V., D.J., E.B.), Johns Hopkins University School of Medicine, Baltimore, MD; and Department of Cardiology (D.J.), Medical University of South Carolina, Charleston.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Link

https://www.neurology.org/doi/pdfdirect/10.1212/WNL.0000000000207158

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