Associated Papers
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes.
Fan Q et al.
Nature Communications, 2023
37696869 (PubMed )
Supplement: 41467_2023_41256_MOESM3_ESM.xlsx › Supplementary_Data_9
A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations.
Jayadev R et al.
Science Advances, 2022
35584218 (PubMed )
Supplement: sciadv.abn2265_sm.pdf
Case report: Genetic defects in laminin α5 cause infantile steroid-resistant nephrotic syndrome.
Sunwoo Y et al.
Frontiers in Pediatrics, 2022
Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome.
Taniguchi Y et al.
Kidney360, 2021
Genetic Dissection of Hypertrophic Cardiomyopathy with Myocardial RNA-Seq.
Gao J et al.
International Journal of Molecular Sciences, 2020
32344918 (PubMed )
Supplement: ijms-21-03040-s001.zip › Supplementary_Data › Supplementary_Data_2.xlsx › S_Data_2
Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
Braun DA et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2019
Select a paper to view details