Cargando…
PACS1-Neurodevelopmental disorder: clinical features and trial readiness
BACKGROUND: PACS1-Neurodevelopmental Disorder (PACS1-NDD) is an ultra-rare condition due to a recurrent mutation in the PACS1 gene. Little systematically collected data exist about the functional abilities and neurodevelopmental morbidities in children with PACS1-NDD METHODS: Parents of individuals...
Autores principales: | Van Nuland, Abigail, Reddy, Taruna, Quassem, Farhad, Vassalli, Jean-Dominique, Berg, Anne T. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438988/ https://www.ncbi.nlm.nih.gov/pubmed/34517877 http://dx.doi.org/10.1186/s13023-021-02001-1 |
Ejemplares similares
-
A Novel Multi-Exon Deletion of PACS1 in a Three-Generation Pedigree: Supplements to PACS1 Neurodevelopmental Disorder Spectrum
por: Liu, Yuan, et al.
Publicado: (2021) -
Heart Disease Characterization and Myocardial Strain Analysis in Patients with PACS1 Neurodevelopmental Disorder
por: Latorre-Pellicer, Ana, et al.
Publicado: (2023) -
Schuurs–Hoeijmakers Syndrome (PACS1 Neurodevelopmental Disorder): Seven Novel Patients and a Review
por: Tenorio-Castaño, Jair, et al.
Publicado: (2021) -
PAC in FACTT: Time to PAC it in?
por: Mansour, Wissam, et al.
Publicado: (2008) -
Transcription Pause and Escape in Neurodevelopmental Disorders
por: Eigenhuis, Kristel N., et al.
Publicado: (2022)