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Co-Occurring Heterozygous CNOT3 and SMAD6 Truncating Variants: Unusual Presentation and Refinement of the IDDSADF Phenotype
Objective, the application of genomic sequencing in clinical practice has allowed us to appreciate the contribution of co-occurring pathogenic variants to complex and unclassified clinical phenotypes. Besides the clinical relevance, these findings have provided evidence of previously unrecognized fu...
Autores principales: | Priolo, Manuela, Radio, Francesca Clementina, Pizzi, Simone, Pintomalli, Letizia, Pantaleoni, Francesca, Mancini, Cecilia, Cordeddu, Viviana, Africa, Emilio, Mammì, Corrado, Dallapiccola, Bruno, Tartaglia, Marco |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303239/ https://www.ncbi.nlm.nih.gov/pubmed/34208845 http://dx.doi.org/10.3390/genes12071009 |
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