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Academic Article
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Continuant
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Entity
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56637967
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relates: Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD

Generically Dependent Continuant
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Article
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RDF description of Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD - http://irises.unilink.it/resource/item/87694
rights: termsOfUse
date: 2026-08-26T01:37:23
publisher: Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD
type: Document

Information Content Entity
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Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD
type: Academic Article
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language: Inglese
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most specific type: Academic Article
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related by: 56637967
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type: Article

Inglese
type: Language