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Journal: Genes, 2022
Volume: 13
Number: 2358

Article: Congenital Defects in a Patient Carrying a Novel Homozygous AEBP1 Variant: Further Expansion of the Phenotypic Spectrum of Ehlers–Danlos Syndrome Classical-like Type 2?
Authors: by Niccolò Di Giosaffatte, Alessandro Ferraris, Federica Gaudioso, Valentina Lodato, Emanuele Savino, Claudia Celletti, Filippo Camerota, Simone Bargiacchi, Luigi Laino, Silvia Majore, Irene Bottillo and Paola Grammatico
Link: https://www.mdpi.com/2073-4425/13/12/2358

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