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Ritelli, M. et al. (2020). Identification of the novel COL5A1 c.3369_3431dup, p.(Glu1124_Gly1144dup) variant in a patient with incomplete classical Ehlers–Danlos syndrome: The importance of phenotype‐guided genetic testing. Molecular genetics & genomic medicine. 8 (10), p. n/a. [Online].