Glomerulopathy associated with predominant fibronectin deposits: Exclusion of the genes for fibronectin, villin and desmin as causative genes
- 3 May 1996
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 63 (1), 323-327
- https://doi.org/10.1002/(sici)1096-8628(19960503)63:1<323::aid-ajmg54>3.0.co;2-m
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Glomerulopathy associated with predominant fibronectin deposits: A newly recognized hereditary diseaseKidney International, 1995
- Genetic renal diseases in childrenCurrent Opinion in Pediatrics, 1995
- Integrated human genome–wide maps constructed using the CEPH reference panelNature Genetics, 1994
- Report of the Third International Workshop on Human Chromosome 2 Mapping 1994Cytogenetic and Genome Research, 1994
- An RFLP map for 2q33‐q37 from multicase mycobacterial and leishmanial disease families: no evidence for an Lsh/Ity/Bcg gene homologue influencing susceptibility to leprosyAnnals of Human Genetics, 1993
- A Comprehensive Genetic Linkage Map of the Human GenomeScience, 1992
- Glomerulonephritis with organized deposits: A mesangiopathic, not immune complex-mediated disease? A pathologic study of two cases in the same familyHuman Pathology, 1992
- Familial lobular glomerulopathyHuman Pathology, 1991
- Familial glomerulopathy with giant fibrillar depositsVirchows Archiv, 1980