Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. (Q50356644)
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scientific article published on 23 September 2013
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English | Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. |
scientific article published on 23 September 2013 |
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Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. (English)
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M Sommen
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C Claes
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J Pinner
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M Flaherty
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F Collins
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23 September 2013
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86
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3
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282-286
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