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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2010-2-24
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pubmed:abstractText |
The purposes of this study were to describe the clinical characteristics of corneal patients with mutations in the SLC4A11 gene and to determine if these characteristics could be correlated with specific genetic mutations.
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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:month |
Mar
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pubmed:issn |
1536-4798
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
302-6
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pubmed:meshHeading |
pubmed-meshheading:20118786-Adolescent,
pubmed-meshheading:20118786-Anion Transport Proteins,
pubmed-meshheading:20118786-Antiporters,
pubmed-meshheading:20118786-Audiometry,
pubmed-meshheading:20118786-Child,
pubmed-meshheading:20118786-Child, Preschool,
pubmed-meshheading:20118786-Corneal Dystrophies, Hereditary,
pubmed-meshheading:20118786-Endothelium, Corneal,
pubmed-meshheading:20118786-Female,
pubmed-meshheading:20118786-Genotype,
pubmed-meshheading:20118786-Hearing Loss, Sensorineural,
pubmed-meshheading:20118786-Humans,
pubmed-meshheading:20118786-Keratoplasty, Penetrating,
pubmed-meshheading:20118786-Male,
pubmed-meshheading:20118786-Mutation,
pubmed-meshheading:20118786-Pedigree,
pubmed-meshheading:20118786-Phenotype,
pubmed-meshheading:20118786-Retrospective Studies,
pubmed-meshheading:20118786-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:20118786-Young Adult
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pubmed:year |
2010
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pubmed:articleTitle |
Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene.
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pubmed:affiliation |
Singapore National Eye Centre, Singapore. jodmehta@gmail.com
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pubmed:publicationType |
Journal Article
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