SLC39A13 and Ehlers-Danlos syndrome: ZIP13-deficient mice have abnormal systemic and bone growth with characteristics reminiscent of human Ehlers-Danlos syndrome (EDS), a group of recessive genetic disorders that affect connective tissue development, and of Osteogenesis Imperfecta, formally named as Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS, OMIM 612350) [30–35].