|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0015576,
umls-concept:C0017398,
umls-concept:C0019904,
umls-concept:C0030567,
umls-concept:C0238604,
umls-concept:C0239307,
umls-concept:C0314657,
umls-concept:C0752099,
umls-concept:C1257890,
umls-concept:C1442161,
umls-concept:C1513822,
umls-concept:C1537041,
umls-concept:C1556084,
umls-concept:C1880171,
umls-concept:C2603343
|
|
pubmed:issue |
9137
|
|
pubmed:dateCreated |
1998-11-17
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Oct
|
|
pubmed:issn |
0140-6736
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
24
|
|
pubmed:volume |
352
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1355-6
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:9802278-Adolescent,
pubmed-meshheading:9802278-Adult,
pubmed-meshheading:9802278-Algeria,
pubmed-meshheading:9802278-Child,
pubmed-meshheading:9802278-Europe,
pubmed-meshheading:9802278-Exons,
pubmed-meshheading:9802278-Female,
pubmed-meshheading:9802278-Gene Deletion,
pubmed-meshheading:9802278-Humans,
pubmed-meshheading:9802278-Male,
pubmed-meshheading:9802278-Middle Aged,
pubmed-meshheading:9802278-Parkinson Disease,
pubmed-meshheading:9802278-Phenotype
|
|
pubmed:year |
1998
|
|
pubmed:articleTitle |
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group.
|
|
pubmed:publicationType |
Letter,
Research Support, Non-U.S. Gov't
|
