Source:http://linkedlifedata.com/resource/pubmed/id/16847948
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
2006-11-1
|
| pubmed:commentsCorrections | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Oct
|
| pubmed:issn |
0364-5134
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
60
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
485; author reply 485-6
|
| pubmed:meshHeading |
pubmed-meshheading:16847948-Ataxia,
pubmed-meshheading:16847948-Child,
pubmed-meshheading:16847948-Guanine Nucleotide Exchange Factors,
pubmed-meshheading:16847948-Hereditary Central Nervous System Demyelinating Diseases,
pubmed-meshheading:16847948-Humans,
pubmed-meshheading:16847948-Myelin Sheath,
pubmed-meshheading:16847948-Syndrome
|
| pubmed:year |
2006
|
| pubmed:articleTitle |
Autosomal dominant leukodystrophy and childhood ataxia with central nervous system hypomyelination syndrome.
|
| pubmed:publicationType |
Letter,
Comment
|