Associated Papers
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.
Matejas V et al.
Human Mutation, 2010
Ophthalmological aspects of Pierson syndrome.
Bredrup C et al.
American Journal of Ophthalmology, 2008
Neurodevelopmental deficits in Pierson (microcoria-congenital nephrosis) syndrome.
Wühl E et al.
American Journal of Medical Genetics. Part A, 2007
Select a paper to view details