Bull terrier hereditary nephritis: a model for autosomal dominant Alport syndrome.

No abstract is available for this paper.

• Publication year

  1995

• Venue

  Kidney International

• Publication date

  1995-03-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1038/KI.1995.116PMID 7752574
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• KCTD1 and Scalp-Ear-Nipple (‘Finlay–Marks’) syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains

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• Transplantation of umbilical cord mesenchymal stem cells into mice with focal segmental glomerulosclerosis delayed disease manifestation.

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• Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?

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