Genotype‐phenotype correlation and prognostic impact in Chinese patients with Alport Syndrome

BACKGROUND: Alport Syndrome (AS) is a progressive hereditary glomerular disease. It is often accompanied by sensorineural hearing loss and ocular abnormalities and can sometimes develop into end stage renal disease (ESRD), which is caused by mutations in the genes encoding the collagen type IV famil...

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Detalles Bibliográficos
Autores principales: Shang, Shunlai, Peng, Fei, Wang, Tao, Wu, Xiaoyuan, Li, Ping, Li, Qinggang, Chen, Xiang M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625365/
https://www.ncbi.nlm.nih.gov/pubmed/31144478
http://dx.doi.org/10.1002/mgg3.741

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625365/
https://www.ncbi.nlm.nih.gov/pubmed/31144478
http://dx.doi.org/10.1002/mgg3.741

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