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The EDS spondylodysplastic type (group D: disorders of glycosaminoglycan biosynthesis) is either caused by homozygous or compound heterozygous mutations in the B4GALT7 gene on chromosome 5q35, or by mutations in the B3GALT6 gene (galactosytransferases) (OMIM # 615349) or in the SLC39A13 gene (zinc transporter) (OMIM # 612350) [2, 3]

Enhancer dissection by Cas9-mediated in situ saturating mutagenesis

This research project has been funded by the Open University and the Research England Expanding Excellence in England 124.18

Peptides in this space can fall under prohibited categories in regulated sport, and status changes over time