Molecular mechanisms and clinical manifestations of rare genetic disorders associated with type I collagen (2019) https://t.co/RKbDi5MwhL

"The sTNX concentrations in half of the JHS/hEDS patients were significantly lower than those in healthy individuals....[But NO TNXB mutations!] These results indicate that the decrease in sTNX concentration could be used as a risk factor for JHS/hEDS." https://t.co/6slFRuWy1e