Associated Papers
Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families.
McKenzie F et al.
Clinical Genetics, 2021
A flexible computational pipeline for research analyses of unsolved clinical exome cases.
Lassmann T et al.
Npj Genomic Medicine, 2020
33303739 (PubMed )
Supplement: 41525_2020_161_MOESM2_ESM.xlsx › Table_S2_03Jun20_SNG
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