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Updated: Jan 1, 2026

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Galloping tongue syndrome in a PRRT2 mutation carrier
Dolores Vilas1, Anna Marcé-Grau1, Alfons Macaya1
1Parkinson's Disease and Movement Disorders Unit (D.V., E.T.), Neurology Service, ICN, Hospital Clínic, University of Barcelona, Spain; Pediatric Neurology Research Group (A.M.-G., A.M.), Vall d'Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona, Spain; Electrophysiology Unit (J.V.-S.), Neurology Service, ICN, Hospital Clinic, University of Barcelona, Spain; Institut August Pi I Sunyer Biomedical Research Institute (IDIBAPS) (J.V.-S., E.T.).
No abstract available in PubMed .
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