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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Genet Genomic Med
Prif Awduron: Shang, Shunlai, Peng, Fei, Wang, Tao, Wu, Xiaoyuan, Li, Ping, Li, Qinggang, Chen, Xiang M.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: John Wiley and Sons Inc. 2019
Pynciau:
Original Articles
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6625365/
https://ncbi.nlm.nih.gov/pubmed/31144478
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.741
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