Comprehensive strategy improves the genetic diagnosis of different polycystic kidney diseases

Polycystic kidney disease (PKD) is known to occur in three main forms, namely autosomal dominant PKD (ADPKD), autosomal recessive PKD (ARPKD) and syndromic PKD (SPKD), based on the clinical manifestations and genetic causes, which are diagnosable from the embryo stage to the later stages of life. Se...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Hua‐Ying, Zhang, Jing, Qiu, Wei, Liang, Chao, Li, Cun‐Xi, Wei, Tian‐Ying, Feng, Zhan‐Ke, Guo, Qing, Yang, Kai, Liu, Zu‐Guo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256360/
https://www.ncbi.nlm.nih.gov/pubmed/34032358
http://dx.doi.org/10.1111/jcmm.16608

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256360/
https://www.ncbi.nlm.nih.gov/pubmed/34032358
http://dx.doi.org/10.1111/jcmm.16608

Ejemplares similares