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- 1750-1172-9-55 doi "10.1186/1750-1172-9-55".
- 1750-1172-9-55 isCitedBy EPS8.
- 1750-1172-9-55 issue "1".
- 1750-1172-9-55 journal "Orphanet Journal of Rare Diseases".
- 1750-1172-9-55 pages "55".
- 1750-1172-9-55 pmc "4022326".
- 1750-1172-9-55 pmid "24741995".
- 1750-1172-9-55 title "EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness".
- 1750-1172-9-55 vauthors "Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C".
- 1750-1172-9-55 volume "9".
- 1750-1172-9-55 year "2014".