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.

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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

Rare

Publisher

Elsevier

Publication Date

01/11/2024

Keywords

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