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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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I publikationen: | Clin J Am Soc Nephrol |
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Huvudupphovsmän: | , , , , , , , , , , , , , , , , |
Materialtyp: | Artigo |
Språk: | Inglês |
Publicerad: |
American Society of Nephrology
2016
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Ämnen: | |
Länkar: | 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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