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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2006-11-14
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pubmed:databankReference |
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pubmed:abstractText |
To refine the interval for X-linked congenital idiopathic nystagmus at Xq24-q26.3 and to evaluate a novel candidate gene (Muscleblind-like 3 gene [MBNL3]).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1090-0535
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1211-6
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pubmed:meshHeading |
pubmed-meshheading:17102799-Chromosome Mapping,
pubmed-meshheading:17102799-Chromosomes, Human, X,
pubmed-meshheading:17102799-DNA Mutational Analysis,
pubmed-meshheading:17102799-Female,
pubmed-meshheading:17102799-Genes, Recessive,
pubmed-meshheading:17102799-Genes, X-Linked,
pubmed-meshheading:17102799-Humans,
pubmed-meshheading:17102799-Lod Score,
pubmed-meshheading:17102799-Male,
pubmed-meshheading:17102799-Microsatellite Repeats,
pubmed-meshheading:17102799-Nystagmus, Congenital,
pubmed-meshheading:17102799-Pedigree,
pubmed-meshheading:17102799-RNA-Binding Proteins
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pubmed:year |
2006
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pubmed:articleTitle |
Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.
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pubmed:affiliation |
Clinical Neurosciences Division, University of Southampton, Southampton, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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