Matches in DBpedia 2016-04 for { <http://doi.org/10.1212/01.wnl.0000182813.94713.ee> ?p ?o }
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- 01.wnl.0000182813.94713.ee author "Zanni G".
- 01.wnl.0000182813.94713.ee author2 "Saillour Y".
- 01.wnl.0000182813.94713.ee author3 "Nagara M".
- 01.wnl.0000182813.94713.ee displayAuthors "3".
- 01.wnl.0000182813.94713.ee doi "10.1212/01.wnl.0000182813.94713.ee".
- 01.wnl.0000182813.94713.ee first4 "P".
- 01.wnl.0000182813.94713.ee first5 "L".
- 01.wnl.0000182813.94713.ee first6 "C".
- 01.wnl.0000182813.94713.ee first7 "L".
- 01.wnl.0000182813.94713.ee first8 "E".
- 01.wnl.0000182813.94713.ee first9 "A".
- 01.wnl.0000182813.94713.ee isCitedBy OPHN1.
- 01.wnl.0000182813.94713.ee issue "9".
- 01.wnl.0000182813.94713.ee journal "Neurology".
- 01.wnl.0000182813.94713.ee last4 "Billuart".
- 01.wnl.0000182813.94713.ee last5 "Castelnau".
- 01.wnl.0000182813.94713.ee last6 "Moraine".
- 01.wnl.0000182813.94713.ee last7 "Faivre".
- 01.wnl.0000182813.94713.ee last8 "Bertini".
- 01.wnl.0000182813.94713.ee last9 "Durr".
- 01.wnl.0000182813.94713.ee nameListFormat "vanc".
- 01.wnl.0000182813.94713.ee pages "1364–9".
- 01.wnl.0000182813.94713.ee pmid "16221952".
- 01.wnl.0000182813.94713.ee title "Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia".
- 01.wnl.0000182813.94713.ee volume "65".
- 01.wnl.0000182813.94713.ee year "2006".