Screening of Fabry disease in patients with chronic kidney disease in Japan

BACKGROUND: Fabry disease (FD), an X-linked lysosomal storage disorder caused by a deficiency in alfa-galactosidase A (α-Gal A) activity due to mutations in the GLA gene, has a prevalence of 0–1.69% in patients undergoing haemodialysis; however, its prevalence in patients with chronic kidney disease...

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Detalles Bibliográficos
Autores principales: Nagata, Akiko, Nasu, Makoto, Kaida, Yusuke, Nakayama, Yosuke, Kurokawa, Yuka, Nakamura, Nao, Shibata, Ryo, Hazama, Takuma, Tsukimura, Takahiro, Togawa, Tadayasu, Saito, Seiji, Sakuraba, Hitoshi, Fukami, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719579/
https://www.ncbi.nlm.nih.gov/pubmed/34282462
http://dx.doi.org/10.1093/ndt/gfaa324

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719579/
https://www.ncbi.nlm.nih.gov/pubmed/34282462
http://dx.doi.org/10.1093/ndt/gfaa324

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