Source:http://linkedlifedata.com/resource/pubmed/id/18080847
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
2008-3-26
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0340-5354
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
255
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
456-8
|
pubmed:meshHeading |
pubmed-meshheading:18080847-Alleles,
pubmed-meshheading:18080847-Brain,
pubmed-meshheading:18080847-Child,
pubmed-meshheading:18080847-Corneal Dystrophies, Hereditary,
pubmed-meshheading:18080847-Female,
pubmed-meshheading:18080847-Humans,
pubmed-meshheading:18080847-Magnetic Resonance Imaging,
pubmed-meshheading:18080847-Repetitive Sequences, Nucleic Acid,
pubmed-meshheading:18080847-Spinocerebellar Ataxias,
pubmed-meshheading:18080847-Syndrome
|
pubmed:year |
2008
|
pubmed:articleTitle |
Spinocerebellar ataxia type 7 presenting as Stargardt's disease.
|
pubmed:publicationType |
Letter,
Case Reports
|