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2016年學術文章 vědecký článek vetenskaplig artikel artikull shkencor vitskapeleg artikkel scientific article published on 3 February 2016 2016年学术文章 επιστημονικό άρθρο bilimsel makale artigo científico 2016年学术文章 2016年學術文章 2016 nî lūn-bûn vitenskapelig artikkel bài báo khoa học articol științific artículo científico publicado en 2016 2016年學術文章 სამეცნიერო სტატია wetenschappelijk artikel artigo científico vedecký článok научная статья tudományos cikk наукова стаття, опублікована в лютому 2016 ৩ ফেব্রুয়ারি ২০১৬-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ article scientifique 2016年学术文章 2016年学术文章 tieteellinen artikkeli wissenschaftlicher Artikel naučni članak מאמר מדעי videnskabelig artikel scienca artikolo artigo científico articolo scientifico 2016年學術文章 2016年の論文 article scientific artykuł naukowy artikulong pang-agham artikel ilmiah บทความทางวิทยาศาสตร์ научни чланак artículu científicu 2016年學術文章 2016年学术文章 scientific article published on 3 February 2016 научна статия 2016 թվականի փետրվարի 3-ին հրատարակված գիտական հոդված научни чланак scientific article published on 3 February 2016 2016年学术文章 article científic мақолаи илмӣ teaduslik artikkel 2016년 논문 مقالة علمية نشرت في 3 فبراير 2016
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Janine Altmüller Claudia Krause Jens Schallner Teresa Neuhann Wolfgang Berger Barbora Novotna Anne-Karin Kahlert Karl Hackmann Holger Thiele Andrea Bier Shawn E Parnell Evelin Schrock Irmingard Neuhann Ian A Glass Anke M Nissen Anna Benet-Pages
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Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt.
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Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt.
schema:name
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt.
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Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt
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