Exclusion of the uteroglobin gene as a candidate f... [Nephrol Dial Transplant. 1998]

Cited by 2 PubMed Central articles

Mutations in FN1 cause glomerulopathy with fibronectin deposits.
Castelletti F, Donadelli R, Banterla F, Hildebrandt F, Zipfel PF, Bresin E, Otto E, Skerka C, Renieri A, Todeschini M, et al. Proc Natl Acad Sci U S A. 2008 Feb 19; 105(7):2538-43. Epub 2008 Feb 11.

[Proc Natl Acad Sci U S A. 2008]
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.
Vollmer M, Jung M, Rüschendorf F, Ruf R, Wienker T, Reis A, Krapf R, Hildebrandt F. Am J Hum Genet. 1998 Dec; 63(6):1724-31.

[Am J Hum Genet. 1998]

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