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HARVARD Citation
Syx, D. et al. (2019). Bi-allelic AEBP1 mutations in two patients with Ehlers–Danlos syndrome. Human molecular genetics. pp. 1853-1864. [Online].
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Syx, D. et al. (2019). Bi-allelic AEBP1 mutations in two patients with Ehlers–Danlos syndrome. Human molecular genetics. pp. 1853-1864. [Online].