Associated Papers
The clinical characteristics and genotype analysis of LAMB2 gene mutation.
Li G et al.
Frontiers in Medicine, 2024
Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease.
Suzuki R et al.
Kidney International Reports, 2023
37705905 (PubMed )
Supplement: mmc1.pdf
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.
Matejas V et al.
Human Mutation, 2010
Variable phenotype of Pierson syndrome.
Choi HJ et al.
Pediatric Nephrology (berlin, Germany), 2008
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