. . . "artigo cient\u00EDfico"@gl . . . . . . "nau\u010Dni \u010Dlanak"@sr-el . "teaduslik artikkel"@et . . "2007\u5E74\u8BBA\u6587"@zh . "121" . "scientific article"@en . . . . "\u043D\u0430\u0443\u0447\u043D\u0430\u044F \u0441\u0442\u0430\u0442\u044C\u044F"@ru . . "\u043D\u0430\u0443\u043A\u043E\u0432\u0430 \u0441\u0442\u0430\u0442\u0442\u044F, \u043E\u043F\u0443\u0431\u043B\u0456\u043A\u043E\u0432\u0430\u043D\u0430 \u0443 \u043A\u0432\u0456\u0442\u043D\u0456 2007"@uk . "tudom\u00E1nyos cikk"@hu . . . . . "\u0633\u0627\u0626\u0646\u0633\u06CC \u0645\u0636\u0645\u0648\u0646"@ur . "wetenschappelijk artikel (gepubliceerd in 2007-04)"@nl . . . . "2007\u5E74\u8AD6\u6587"@zh-hant . . . . "\u043D\u0430\u0443\u0447\u043D\u0438 \u0447\u043B\u0430\u043D\u0430\u043A (\u043E\u0431\u0458\u0430\u0432\u0459\u0435\u043D 2007-04)"@sr . . . "\u043D\u0430\u0443\u0447\u043D\u0438 \u0447\u043B\u0430\u043D\u0430\u043A"@sr-ec . "2007\u5E74\u8AD6\u6587"@yue . "1032710328" . "mokslinis straipsnis"@lt . . "vedeck\u00FD \u010Dl\u00E1nok (publikovan\u00FD 2007-04)"@sk . "art\u00EDculu cient\u00EDficu espubliz\u00E1u en 2007"@ast . "tieteellinen artikkeli"@fi . . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@en-gb . . "\u043C\u0430\u049B\u043E\u043B\u0430\u0438 \u0438\u043B\u043C\u04E3"@tg . . "2007 \u0569\u0578\u0582\u0561\u056F\u0561\u0576\u056B \u0531\u057A\u0580\u056B\u056C\u056B\u0576 \u0570\u0580\u0561\u057F\u0561\u0580\u0561\u056F\u0578\u0582\u0561\u056E \u0563\u056B\u057F\u0561\u056F\u0561\u0576 \u0575\u0585\u0564\u0578\u0582\u0561\u056E"@hyw . "\u0645\u0642\u0627\u0644\u0647\u0654 \u0639\u0644\u0645\u06CC"@fa . "artikulong pang-agham"@tl . "artigo cient\u00EDfico (publicado na 2007-04)"@pt . . "\u10E1\u10D0\u10DB\u10D4\u10EA\u10DC\u10D8\u10D4\u10E0\u10DD \u10E1\u10E2\u10D0\u10E2\u10D8\u10D0"@ka . "2007\u5E74\u8AD6\u6587"@zh-hk . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@en . "\u09E8\u09E6\u09E6\u09ED-\u098F \u09AA\u09CD\u09B0\u0995\u09BE\u09B6\u09BF\u09A4 \u09AC\u09C8\u099C\u09CD\u099E\u09BE\u09A8\u09BF\u0995 \u09A8\u09BF\u09AC\u09A8\u09CD\u09A7"@bn . . "Hanno Bolz" . . "wissenschaftlicher Artikel (ver\u00F6ffentlicht in April 2007)"@de . "videnskabelig artikel (udgivet 2007-04)"@da . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@en . "Jos\u00E9 M Mill\u00E1n" . . "2007\u5E74\u8BBA\u6587"@wuu . "v\u011Bdeck\u00FD \u010Dl\u00E1nek publikovan\u00FD v roce 2007"@cs . . . . . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@en-gb . "article scientific"@oc . "artigo cient\u00EDfico (publicado na 2007)"@pt-br . . "2007 n\u00EE l\u016Bn-b\u00FBn"@nan . "artyku\u0142 naukowy"@pl . . "vitskapeleg artikkel"@nn . "2007\u5E74\u8BBA\u6587"@zh-cn . . . "2007\u5E74\u8BBA\u6587"@zh-sg . . . . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@ast . "6627636" . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@en-gb . . . . . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@en . . . "2007 \u0569\u057E\u0561\u056F\u0561\u0576\u056B \u0561\u057A\u0580\u056B\u056C\u056B\u0576 \u0570\u0580\u0561\u057F\u0561\u0580\u0561\u056F\u057E\u0561\u056E \u0563\u056B\u057F\u0561\u056F\u0561\u0576 \u0570\u0578\u0564\u057E\u0561\u056E"@hy . . "article cient\u00EDfic"@ca . . "vetenskaplig artikel"@sv . . . . . . . . . . . "vitenskapelig artikkel"@nb . "2007\u5E74\u8AD6\u6587"@zh-mo . "Bernhard Jurklies" . . "J\u00FCrgen Lamprecht" . "b\u00E0i b\u00E1o khoa h\u1ECDc"@vi . . . "\u043C\u0430\u049B\u043E\u043B\u0430\u0438 \u0438\u043B\u043C\u04E3"@tg-cyrl . "\u05DE\u05D0\u05DE\u05E8 \u05DE\u05D3\u05E2\u05D9"@he . . . . . . . "\u043D\u0430\u0443\u0447\u043D\u0430 \u0441\u0442\u0430\u0442\u0438\u044F"@bg . "2006-12-15T00:00:00Z"^^ . . . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@nl . "2" . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@en . . . "articolo scientifico (pubblicato il 2007-04)"@it . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@ast . . "2007\u5E74\u8AD6\u6587"@zh-tw . . . . . "scienca artikolo"@eo . "\u03B5\u03C0\u03B9\u03C3\u03C4\u03B7\u03BC\u03BF\u03BD\u03B9\u03BA\u03CC \u03AC\u03C1\u03B8\u03C1\u03BF"@el . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@ast . . "17171570" . "2163829" . "article scientifique (publi\u00E9 2007-04)"@fr . . "art\u00EDculo cient\u00EDfico publicado en 2007"@es . "articol \u0219tiin\u021Bific"@ro . "10.1007/S00439-006-0304-0" . "\u0645\u0642\u0627\u0644\u0629 \u0639\u0644\u0645\u064A\u0629 (\u0646\u0634\u0631\u062A \u0641\u064A \u0623\u0628\u0631\u064A\u0644 2007)"@ar . "bilimsel makale"@tr . "2007\u5E74\u8BBA\u6587"@zh-my . "\u0E1A\u0E17\u0E04\u0E27\u0E32\u0E21\u0E17\u0E32\u0E07\u0E27\u0E34\u0E17\u0E22\u0E32\u0E28\u0E32\u0E2A\u0E15\u0E23\u0E4C"@th . . . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@nl . . . "Elena Aller" . . "Inga Ebermann" . . "203-211" . "2007\uB144 \uB17C\uBB38"@ko . . "artikull shkencor"@sq . . . . . . "2007\u5E74\u306E\u8AD6\u6587"@ja . "2007\u5E74\u8BBA\u6587"@zh-hans . "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss"@nl . "release_6pj4trdspzdhdeqas4gwfafb3u" . .