Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Porencephaly type 2 is an autosomal dominant disease caused by mutations of the COL4A2 gene.
| 1. |
Yoneda Y et al. (2012) De novo and inherited mutations in COL4A2, encoding the type IV collagen α2 chain cause porencephaly. 
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| 2. |
OMIM.ORG article Omim 614483
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