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FBXW7-Related Neurodevelopmental Disorder: Clinical Spectrum, Molecular Mechanisms, and Tumor Predisposition.

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Title: FBXW7-Related Neurodevelopmental Disorder: Clinical Spectrum, Molecular Mechanisms, and Tumor Predisposition.
Authors: Savasta S; Pediatric Clinic and Rare Diseases, Microcitemico Hospital 'A. Cao', University of Cagliari, Cagliari, Italy, unica.it.; Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy, unica.it., Comisi FF; Pediatric Clinic and Rare Diseases, Microcitemico Hospital 'A. Cao', University of Cagliari, Cagliari, Italy, unica.it., Fiumicelli E; Department of Pediatrics, University of Perugia, Perugia, Italy, unipg.it., Dell'Isola GB; Saint Camillus International University of Health Sciences, Rome, Italy.; Department of Developmental Disabilities, IRCCS San Raffaele Roma, Rome, Italy., Di Pasquale G; Department of Pediatrics, University of L'Aquila, L'Aquila, Italy, univaq.it., Mangano GD; Department of Medicine and Surgery, University of Enna Kore, Enna, Italy, unikore.it., Zagaroli L; Department of Pediatrics, University of L'Aquila, L'Aquila, Italy, univaq.it., Salpietro V; Department of Pediatrics, University of L'Aquila, L'Aquila, Italy, univaq.it.; European Brain Research Institute (EBRI) 'Rita Levi-Montalcini', Rome, Italy, ebri.it., Verrotti A; Department of Pediatrics, University of Perugia, Perugia, Italy, unipg.it.
Source: Human mutation [Hum Mutat] 2026 May 08; Vol. 2026, pp. 3764750. Date of Electronic Publication: 2026 May 08 (Print Publication: 2026).
Publication Type: Journal Article; Review
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1098-1004
DOI:10.1155/humu/3764750