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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8906
|
pubmed:dateCreated |
1994-6-10
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0140-6736
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
7
|
pubmed:volume |
343
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1111-2
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:7910226-Charcot-Marie-Tooth Disease,
pubmed-meshheading:7910226-Chromosomes, Human, Pair 1,
pubmed-meshheading:7910226-Chromosomes, Human, Pair 17,
pubmed-meshheading:7910226-Connexins,
pubmed-meshheading:7910226-Humans,
pubmed-meshheading:7910226-Mutation,
pubmed-meshheading:7910226-X Chromosome
|
pubmed:year |
1994
|
pubmed:articleTitle |
CMTX1: a gap junction genetic disease.
|
pubmed:affiliation |
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY.
|
pubmed:publicationType |
Journal Article
|