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This group only suggests such treatment when IGF-1 deficiency prevails, acting merely as a substitutive therapy, and never to exploit its multiple actions
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Mutations in the COL5A1 gene are causal in the EhlersDanlos syndrome I and II
To view a copy of this licence, visit About this article Cite this article Yang, J., He, J
doi: 10.1016/j.eclinm.2023.101826 163 StnderS
