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Statements

Subject Item
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سائنسی مضمون teaduslik artikkel vitskapeleg artikkel bài báo khoa học vetenskaplig artikel videnskabelig artikel (udgivet 2002/12/24) tudományos cikk 2002年论文 article científic 2002년 논문 naučni članak мақолаи илмӣ articolo scientifico (pubblicato il 2002/12/24) 2002年論文 2002年论文 επιστημονικό άρθρο научни чланак 2002年論文 บทความทางวิทยาศาสตร์ vedecký článok (publikovaný 2002/12/24) mokslinis straipsnis artikulong pang-agham 2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած מאמר מדעי artículu científicu espublizáu en 2002 artigo científico (publicado na 2002) научная статья 2002年论文 bilimsel makale مقالة علمية (نشرت في 24-12-2002) wissenschaftlicher Artikel (veröffentlicht am 24 Dezember 2002) tieteellinen artikkeli 2002年论文 2002年論文 artigo científico (publicado na 2002/12/24) სამეცნიერო სტატია 2002年论文 vědecký článek publikovaný v roce 2002 scienca artikolo 2002年の論文 article scientifique (publié 2002/12/24) articol științific artykuł naukowy artikull shkencor wetenschappelijk artikel (gepubliceerd op 2002/12/24) 2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված artigo científico vitenskapelig artikkel scientific article artículo científico publicado en 2002 научна статия 2002年論文 2002 nî lūn-bûn ২০০২-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ مقالهٔ علمی 2002年论文 наукова стаття, опублікована в грудні 2002 2002年論文 мақолаи илмӣ article scientific научни чланак (објављен 2002/12/24)
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wdt:P2093
A Fogli F Deodato A Bartuli O Boespflug-Tanguy
rdfs:label
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
skos:prefLabel
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
schema:name
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
p:P50
wds:Q24337631-733C0BC3-6013-48C9-AE44-2CB8425BBEBA wds:Q24337631-30F4C14E-2B86-4CF2-A7B8-A167E521A40C wds:Q24337631-459D71F4-0F74-49BD-AFA4-2BC86C14A5E1
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p:P1476
wds:Q24337631-803D508C-8F25-49AC-8566-356A6254FE2E
wdt:P1476
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
p:P304
wds:Q24337631-BA7E5D63-2A0E-46C6-9C6B-84AD0CC0A8DB
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1966-8
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n10:01.WNL.0000041666.76863.47
wdt:P356
10.1212/01.WNL.0000041666.76863.47
p:P8608
wds:Q24337631-0700F128-EC13-4922-845E-A0B9CD9E7C06
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release_iy5kbu44hnfyhlgilxpwvggutm