Associated Papers
Exploring unsolved cases of lissencephaly spectrum: integrating exome and genome sequencing for higher diagnostic yield.
Furukawa S et al.
Journal of Human Genetics, 2024
Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing.
Komatsu K et al.
Scientific Reports, 2024
39433808 (PubMed )
Supplement: 41598_2024_75020_MOESM2_ESM.xlsx › Supplementary_Table_S1
Novel LAMC3 pathogenic variant enriched in Finnish population causes malformations of cortical development and severe epilepsy.
Saarela A et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2024
A New Case With Cortical Malformation Caused by Biallelic Variants in LAMC3.
Abe K et al.
Neurology. Genetics, 2022
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