Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene (Q44268960)
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English | Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene |
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Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene (English)
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Cuong D Vu
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Jeremiah Brown
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Jarmo Körkkö
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Robert Ritter
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Albert O Edwards
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1 January 2003
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110
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1
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70-77
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