Linked Life Data

12843336

Source:http://linkedlifedata.com/resource/pubmed/id/12843336

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2003-7-4
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e87
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:12843336-Alternative Splicing, pubmed-meshheading:12843336-Axons, pubmed-meshheading:12843336-Base Sequence, pubmed-meshheading:12843336-Child, pubmed-meshheading:12843336-Codon, Nonsense, pubmed-meshheading:12843336-Consanguinity, pubmed-meshheading:12843336-DNA, pubmed-meshheading:12843336-DNA, Complementary, pubmed-meshheading:12843336-DNA Mutational Analysis, pubmed-meshheading:12843336-Demyelinating Diseases, pubmed-meshheading:12843336-Electrophysiology, pubmed-meshheading:12843336-Family Health, pubmed-meshheading:12843336-Female, pubmed-meshheading:12843336-Genotype, pubmed-meshheading:12843336-Humans, pubmed-meshheading:12843336-Male, pubmed-meshheading:12843336-Microscopy, Electron, pubmed-meshheading:12843336-Mutation, pubmed-meshheading:12843336-Nerve Tissue Proteins, pubmed-meshheading:12843336-Pedigree, pubmed-meshheading:12843336-Peripheral Nervous System Diseases, pubmed-meshheading:12843336-Peroneal Nerve, pubmed-meshheading:12843336-Phenotype
pubmed:year
2003
pubmed:articleTitle
Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations.
pubmed:affiliation
Inserm U491, Génétique Médicale et Développement, Faculté de Médecine la Timone, 13385 Marseille, France.
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't