(Q30332162)
Statements
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Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene. (English)
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Alfons Meindl
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Felix K Jacobi
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Sten Andréasson
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Hana Langrova
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Eberhart Zrenner
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Eckart Apfelstedt-Sylla
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Carsten M Pusch
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21 September 2002
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240
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10
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822-828
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Identifiers
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1 reference