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contentType Journal Article
endingPage 517
issn 0340-6717
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publicationName Human Genetics
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bibliographicCitation Kremer H, Hamel BC, van den Helm B, Arts WF, de Wijs IJ, Sistermans EA, Ropers HH, Mariman EC. 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. Hum Genet. 1996 Nov;98(5):513–7. doi: 10.1007/s004390050250. PMID: 8882866.
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date 1996-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/8882866
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language English
source https://pubmed.ncbi.nlm.nih.gov/
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title 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
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Total number of triples: 37.