Clinical differential factors in patients with hereditary transthyretin amyloidosis with Val142Ile and Ser43Asn mutations

Authors Castellar-Leones Sandra Milena, Ruiz-Ospina Edicson, Diaz-Ruiz Jorge, Correa-Arrieta Cristian, Ruiz-Cortés Xiomara, Luzuriaga-Carpio Diana, Zambrano-Vera Dario, Cedeño-Quincha Jeanneth, Guerrero-Cepeda Luis, César-Chávez Daniel, Ortiz-Corredor Fernando
Journal Orphanet Journal of Rare Diseases
Publication Date 2024-12-20
DOI 10.1186/s13023-024-03496-0

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