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bibliographicCitation Yoshida S, Yamaji Y, Kuwahara R, Yoshida A, Hisatomi T, Ueno A, Ishibashi T. Novel mutation in exon 2 of COL2A1 gene in Japanese family with Stickler Syndrome type I. Eye (Lond). 2006 Jun;20(6):743–5. doi: 10.1038/sj.eye.6702001. PMID: 16021188.
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title Novel mutation in exon 2 of COL2A1 gene in Japanese family with Stickler Syndrome type I
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