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pro vyhledávání: '"Puriya Daniel Würtz Yazdanfard"'
Autor:
Puriya Daniel Würtz Yazdanfard, Grigoris Effraimidis, Christoffer Valdorff Madsen, Lars Holme Nielsen, Åse Krogh Rasmussen, Jørgen Holm Petersen, Søren Schwartz Sørensen, Lars Køber, Vitor Hugo Fraga de Abreu, Vibeke Andrée Larsen, Ulla Feldt-Rasmussen
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100841- (2022)
Background: Fabry disease (FD) is a lysosomal storage disorder resulting in systemic accumulation of globotriaosylceramide (Gb3) causing multi-organ dysfunction. The audiologic involvement in FD has been neglected in previous studies; while not a let
Externí odkaz:
https://doaj.org/article/6cd6ac5f35b14734ab6a47899baa2717
