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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice.
The non-muscle Myosin heavy chain 9 gene (MYH9) is not associated with lupus nephritis in African Americans.
Improving the recognition of hereditary interstitial kidney disease.
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Improving the recognition of hereditary interstitial kidney disease.
Bleyer AJ. Improving the recognition of hereditary interstitial kidney disease. J Am Soc Nephrol. 2009 Jan; 20(1):11-3.
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PubMed
subject areas
Humans
Kidney Diseases
Kidney Diseases, Cystic
Kidney Failure, Chronic
Mucoproteins
Nephritis, Interstitial
authors with profiles
Anthony J. Bleyer MD, MS