Document
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date: 2026-08-24T15:15:40
publisher: Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: A case report
type: Document
label: RDF description of Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: A case report - http://irises.uniss.it/resource/item/122487

Academic Article
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8306707
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relates: Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: A case report

Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: A case report
type: Generically Dependent Continuant
most specific type: Academic Article
language: Inglese
type: Document
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type: Thing
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related by: 8306707

Article
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Inglese
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