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[] [DOI] [PubMed] Wagena EJ, Knipschild PG, Huibers MJH, Wouters EFM, Schayck CPR
N., Park, D
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Most classic EDS (EDS type I and II of the earlier classification) patients harbor heterozygous mutations in the genes encoding for two of the three chains constituting the ubiquitous collagen type V ( COL5A1 and COL5A2 ) [20]
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