Article
De Novo Pathogenic Variant in FBRSL1, Non OMIM Gene Paralogue AUTS2, Causes a Novel Recognizable Syndromic Manifestation with Intellectual Disability; An Additional Patient and Review of the Literature.
Genes - 22 Jun 2024
Bukvic Nenad, De Rinaldis Marta, Chetta Massimiliano, Trabacca Antonio, Bassi Maria Teresa, Marsano René Massimiliano, Holoubkova Lenka, Rivieccio Maria, Oro Maria, Resta Nicoletta, Kerkhof Jennifer, Sadikovic Bekim, Viggiano Luigi
Abstract excerpt
FBRSL1, together with FBRS and AUTS2 (Activator of Transcription and Developmental Regulator; OMIM 607270), constitutes a tripartite AUTS2 gene family. AUTS2 and FBRSL1 are evolutionarily more closely related to each other than to FBRS (Fibrosin 1; OMIM 608601). Despite its paralogous relation to AUTS2, FBRSL1's precise role remains unclear, though it likely shares functions in neurogenesis and transcriptional...
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