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HARVARD Citation
Schrauwen, I. et al. (n.d.). Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. Clinical genetics. pp. 282-286. [Online].
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Schrauwen, I. et al. (n.d.). Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. Clinical genetics. pp. 282-286. [Online].