(Q46822788)
Statements
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Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13. (English)
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A Camuzat
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H Dollfus
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S Gerber
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I Perrault
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J Weissenbach
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A Munnich
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J Kaplan
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1 June 1996
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97
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6
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798-801
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Identifiers
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