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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Dades bibliogràfiques
Publicat a:Clin J Am Soc Nephrol
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: American Society of Nephrology 2016
Matèries:
Original Articles
Accés en línia: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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