Associated Papers
Complex Genetics and Regulatory Drivers of Hypermobile Ehlers-Danlos Syndrome: Insights from Genome-Wide Association Study Meta-analysis.
Petrucci-Nelson T et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Mutational analysis of 12 patients with the phenotype of Ehlers-Danlos syndrome type VIB shows no linkage to the zinc transporter gene SLC39A13.
Walker LC et al.
American Journal of Medical Genetics. Part A, 2011
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