Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Hereditary FSGS type 3 is an autosomal dominant disorder caused by mutations of the CD2AP gene.
| 1. |
Büscher AK et al. (2012) Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients. 
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| 2. |
Kim JM et al. (2003) CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility.
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| 3. |
OMIM.ORG article Omim 607832
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