X-linked recessive nephritis with mental retardation, sensorineural hearing loss, and macrocephaly
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04039.x/fullpdf
Reference20 articles.
1. Hereditary familial congenital haemorrhagic nephritis;Alport;Br J Med,1927
2. Identification of mutations in the COL4A5 collagen gene in Alport syndrome;Barker;Science,1990
3. Major rearrangements in the alpha 5 (IV) collagen gene in three patients with Alport syndrome;Boye;Genomics,1991
4. Diffuse leiomyomatosis in Alport syndrome;Cochat;J Pediatr,1988
5. Ocular changes in the progressive hereditary nephropathies;Dufier;Pediatr Nephrol,1987
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