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An expansion of the phenotype in individuals with SYNCRIP-Related Neurodevelopmental Disorder.

Shafiq T., Feng JL., Phillips L., Murias K., Ferguson M., Baranano K., Acchione A., Kipkemoi P., Kipkoech C., Chepkemoi E., Abubakar A., Newton C., van der Merwe C., O’Heir E., Galvin A., Garcia AG., D’Souza A., Stefanich J., Shillington A., Tuttle A., Torti E., Zhu E., Morsink MAJ., Lebayle E., Corneo B., Ricupero C., Au PYB., Kline AD., Balasubramanian M., Bain J., Gillentine MA.

Original publication

DOI

10.1016/j.rare.2024.100052

Type

Journal article

Journal

Rare

Publisher

Elsevier

Publication Date

01/11/2024

Keywords

31 Biological Sciences, Neurosciences, Mental health, Mental Health, Genetics, Brain Disorders, Minority Health, Autism, Congenital Structural Anomalies, 3105 Genetics, Behavioral and Social Science, Neurodegenerative, 5204 Cognitive and Computational Psychology, 2.1 Biological and endogenous factors, 52 Psychology, Intellectual and Developmental Disabilities (IDD), Pediatric, Clinical Research, Neurological