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Matches in Wikidata for { <http://www.wikidata.org/entity/Q37644432> ?p ?o ?g. }

• Q37644432 description "article científic" @default.
• Q37644432 description "article scientifique" @default.
• Q37644432 description "articolo scientifico" @default.
• Q37644432 description "artigo científico" @default.
• Q37644432 description "artículu científicu espublizáu en 2016" @default.
• Q37644432 description "bilimsel makale" @default.
• Q37644432 description "bài báo khoa học" @default.
• Q37644432 description "scientific article published on 15 December 2016" @default.
• Q37644432 description "vedecký článok" @default.
• Q37644432 description "vetenskaplig artikel" @default.
• Q37644432 description "videnskabelig artikel" @default.
• Q37644432 description "vědecký článek" @default.
• Q37644432 description "wetenschappelijk artikel" @default.
• Q37644432 description "wissenschaftlicher Artikel" @default.
• Q37644432 description "наукова стаття, опублікована в грудні 2016" @default.
• Q37644432 description "научни чланак" @default.
• Q37644432 description "مقالة علمية نشرت في 15 ديسمبر 2016" @default.
• Q37644432 name "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 name "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 name "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 type Item @default.
• Q37644432 label "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 label "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 label "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 prefLabel "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 prefLabel "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
• Q37644432 prefLabel "A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy" @default.
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