Matches in UGent Biblio for { <https://biblio.ugent.be/publication/5846920#aggregation> ?p ?o. }
Showing items 1 to 37 of
37
with 100 items per page.
- aggregation classification "A1".
- aggregation creator B975648.
- aggregation creator B975649.
- aggregation creator B975650.
- aggregation creator B975651.
- aggregation creator B975652.
- aggregation creator B975653.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation date "2015".
- aggregation format "application/pdf".
- aggregation hasFormat 5846920.bibtex.
- aggregation hasFormat 5846920.csv.
- aggregation hasFormat 5846920.dc.
- aggregation hasFormat 5846920.didl.
- aggregation hasFormat 5846920.doc.
- aggregation hasFormat 5846920.json.
- aggregation hasFormat 5846920.mets.
- aggregation hasFormat 5846920.mods.
- aggregation hasFormat 5846920.rdf.
- aggregation hasFormat 5846920.ris.
- aggregation hasFormat 5846920.txt.
- aggregation hasFormat 5846920.xls.
- aggregation hasFormat 5846920.yaml.
- aggregation isPartOf urn:issn:1098-3600.
- aggregation language "eng".
- aggregation rights "I have transferred the copyright for this publication to the publisher".
- aggregation subject "Medicine and Health Sciences".
- aggregation title "Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion".
- aggregation authorList BK1368717.
- aggregation aggregates 5846955.
- aggregation isDescribedBy 5846920.
- aggregation similarTo gim.2014.95.
- aggregation similarTo LU-5846920.