(Q24676361)

English

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

scientific article

Statements

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population (English)
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S Yzer
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L I van den Born
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J Schuil
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H Y Kroes
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M M van Genderen
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F N Boonstra
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B van den Helm
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H G Brunner
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R K Koenekoop
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F P M Cremers
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September 2003
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40
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9
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709-13
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