Clinical and genetic features of AGel amyloidosis caused by novel gelsolin variant and its impact on cardiac function and conduction disorders.

Autor: Roldán-Sevilla A; Inherited Cardiovascular Disease Unit, Cardiology Department, Burgos University Hospital, Spain., Gallego-Delgado M; Inherited Cardiovascular Disease Unit, Department of Cardiology, Complejo Asistencial Universitario de Salamanca, Spain.; CIBER Cardiovascular, Carlos III Health Institute, Madrid, Spain., Lista-Araujo MT; Pathological Anatomy Department, Burgos University Hospital, Burgos, Spain., Torres-Pérez J; Anterior Ophthalmic Segment Unit, Ophthalmology Department, Burgos University Hospital, Burgos, Spain., Merino-Merino AM; Inherited Cardiovascular Disease Unit, Cardiology Department, Burgos University Hospital, Spain., Gil-Polo C; Neurology Department, Burgos University Hospital, Burgos, Spain., Cantero-Lozano D; Electrophisiology Unit, Cardiology Department, Burgos University Hospital, Spain., Lorenzo-Hernandez SM; Laboratory of Molecular Genetics. Clinical Analysis and Clinical Biochemistry Service, Complejo Asistencial Universitario de Salamanca, Spain.; Specific Reference Unit for Pharmacogenetics and Precision Medicine. Rare diseases Reference Unit of Castilla y León (DiERCyL) [AQ]., Eiros-Bachiller R; Inherited Cardiovascular Disease Unit, Department of Cardiology, Complejo Asistencial Universitario de Salamanca, Spain.; CIBER Cardiovascular, Carlos III Health Institute, Madrid, Spain.

Publikováno v: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2024 Dec 19, pp. 1-3. Date of Electronic Publication: 2024 Dec 19.