Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome

BACKGROUND AND OBJECTIVES: Alport syndrome comprises a group of inherited heterogeneous disorders involving CKD, hearing loss, and ocular abnormalities. Autosomal dominant Alport syndrome caused by heterozygous mutations in collagen 4A3 and/or collagen 4A4 accounts for <5% of patients. However, t...

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Detalhes bibliográficos
Publicado no:Clin J Am Soc Nephrol
Main Authors: Kamiyoshi, Naohiro, Nozu, Kandai, Fu, Xue Jun, Morisada, Naoya, Nozu, Yoshimi, Ye, Ming Juan, Imafuku, Aya, Miura, Kenichiro, Yamamura, Tomohiko, Minamikawa, Shogo, Shono, Akemi, Ninchoji, Takeshi, Morioka, Ichiro, Nakanishi, Koichi, Yoshikawa, Norishige, Kaito, Hiroshi, Iijima, Kazumoto
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2016
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4974872/
https://ncbi.nlm.nih.gov/pubmed/27281700
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.01000116
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