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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2007-9-11
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pubmed:abstractText |
To perform a genotype-phenotype correlation study in an X-linked congenital idiopathic nystagmus pedigree (pedigree 1) and to assess the allelic variance of the FRMD7 gene in congenital idiopathic nystagmus.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0003-9950
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
125
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1255-63
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:17846367-Alleles,
pubmed-meshheading:17846367-Cytoskeletal Proteins,
pubmed-meshheading:17846367-Electronystagmography,
pubmed-meshheading:17846367-Eye Movements,
pubmed-meshheading:17846367-Female,
pubmed-meshheading:17846367-Genes, X-Linked,
pubmed-meshheading:17846367-Genetic Diseases, X-Linked,
pubmed-meshheading:17846367-Genetic Linkage,
pubmed-meshheading:17846367-Genetic Variation,
pubmed-meshheading:17846367-Genotype,
pubmed-meshheading:17846367-Humans,
pubmed-meshheading:17846367-Male,
pubmed-meshheading:17846367-Membrane Proteins,
pubmed-meshheading:17846367-Mutation,
pubmed-meshheading:17846367-Nystagmus, Congenital,
pubmed-meshheading:17846367-Pedigree,
pubmed-meshheading:17846367-Phenotype,
pubmed-meshheading:17846367-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:17846367-Sequence Analysis, DNA,
pubmed-meshheading:17846367-X Chromosome Inactivation
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pubmed:year |
2007
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pubmed:articleTitle |
Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus.
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pubmed:affiliation |
Clinical Neurosciences Division, University of Southampton, Southampton, England.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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