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
Laminin β2 variants associated with isolated nephropathy that impact matrix regulation.
Kikkawa Y et al.
Jci Insight, 2021
33749661 (PubMed )
Supplement: jciinsight-6-145908-s063.pdf
Laminin Polymerization and Inherited Disease: Lessons From Genetics.
Shaw L et al.
Frontiers in Genetics, 2021
A Novel Homozygous Truncating Mutation in LAMB2 Gene in a Chinese Uyghur Patient With Severe Phenotype Pierson Syndrome.
Zhu HT et al.
Frontiers in Medicine, 2019
Crystal structures of the network-forming short-arm tips of the laminin β1 and γ1 chains.
Carafoli F et al.
Plos One, 2012
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
A milder variant of Pierson syndrome.
Kagan M et al.
Pediatric Nephrology (berlin, Germany), 2008
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