A carregar...

Contemporary therapeutics and new drug developments for treatment of Fabry disease: a narrative review

Fabry disease (OMIM 301500) is an X-linked (Xq22.1) lysosomal storage disorder leading to a progressive multisystem disease with high variability in both genotype and phenotype expression. The pathophysiological origin is found in an enzyme deficiency of the α-galactosidase A (enzyme commission no....

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Cardiovasc Diagn Ther
Main Authors: Oder, Daniel, Müntze, Jonas, Nordbeck, Peter
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8102271/
https://ncbi.nlm.nih.gov/pubmed/33968645
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/cdt-20-743
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!