A Homozygous Missense COL1A1 Variant (p.Glu684Lys) Associated with an Arthrochalasia-like Ehlers-Danlos Syndrome Phenotype: A Case Report. - Markova T; Melnik E; Kurelev M; Cherevatova T; Nikolaeva A; Gorodilova D; Demina N; Dadali E (Genes, 2026)