RNA Analysis and Clinical Characterization of a Novel Splice Variant in the NSD1 Gene Causing Familial Sotos Syndrome.

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Bibliographic Details
Title: RNA Analysis and Clinical Characterization of a Novel Splice Variant in the NSD1 Gene Causing Familial Sotos Syndrome.
Authors: Villate O; Pediatric Oncology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain., Maortua H; Neurodegenerative Diseases Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.; Genetics Service, Hospital Universitario Cruces-Osakidetza, Barakaldo, Spain., Tejada MI; Genetics Service, Hospital Universitario Cruces-Osakidetza, Barakaldo, Spain.; Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.; Spanish Consortium for Research on Rare Diseases (CIBERER), Madrid, Spain., Llano-Rivas I; Genetics Service, Hospital Universitario Cruces-Osakidetza, Barakaldo, Spain.
Source: Frontiers in pediatrics [Front Pediatr] 2022 Feb 02; Vol. 10, pp. 827802. Date of Electronic Publication: 2022 Feb 02 (Print Publication: 2022).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2296-2360
DOI:10.3389/fped.2022.827802