Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome

INTRODUCTION: X-linked Alport syndrome (XLAS) is a hereditary disease characterized by progressive nephritis, hearing loss, and ocular abnormalities. Affected male patients usually progress to end-stage renal disease in early or middle adulthood, and disease severity is strongly correlated with geno...

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Detalles Bibliográficos
Autores principales: Yamamura, Tomohiko, Nozu, Kandai, Fu, Xue Jun, Nozu, Yoshimi, Ye, Ming Juan, Shono, Akemi, Yamanouchi, Satoko, Minamikawa, Shogo, Morisada, Naoya, Nakanishi, Koichi, Shima, Yuko, Yoshikawa, Norishige, Ninchoji, Takeshi, Morioka, Ichiro, Kaito, Hiroshi, Iijima, Kazumoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733817/
https://www.ncbi.nlm.nih.gov/pubmed/29270492
http://dx.doi.org/10.1016/j.ekir.2017.04.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733817/
https://www.ncbi.nlm.nih.gov/pubmed/29270492
http://dx.doi.org/10.1016/j.ekir.2017.04.011

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