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O'Donnel-Luria-Rodan Syndrome: New gene variant identified in Romania (A case report)
O'Donnel-Luria-Rodan (ODLURO) syndrome is a neurodevelopmental disorder with autosomal dominant inheritance. It appears more frequently in males during the first decade of life and is associated with developmental delay, low intelligence quotient, autism spectrum disorder-like behavior, epileps...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
D.A. Spandidos
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016787/ https://www.ncbi.nlm.nih.gov/pubmed/35481221 http://dx.doi.org/10.3892/etm.2022.11294 |