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Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders
BACKGROUND: We aimed to define the clinical and variant spectrum and to provide novel molecular insights into the DHX30-associated neurodevelopmental disorder. METHODS: Clinical and genetic data from affected individuals were collected through Facebook-based family support group, GeneMatcher, and ou...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140440/ https://www.ncbi.nlm.nih.gov/pubmed/34020708 http://dx.doi.org/10.1186/s13073-021-00900-3 |