(Q50512900)
Statements
Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood. (English)
1 reference
Kremer H
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Hamel BC
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van den Helm B
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Arts WF
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de Wijs IJ
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Sistermans EA
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Ropers HH
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Mariman EC
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1 November 1996
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98
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5
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513-517
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Identifiers
1 reference