Cargando…
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice
Attention-deficit hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder characterized by inattention, impulsivity and hyperactivity. ADHD exhibits substantial heritability, with rare monogenic variants contributing to its pathogenesis. Here we demonstrate familial ADHD cause...
Autores principales: | Halperin, D., Stavsky, A., Kadir, R., Drabkin, M., Wormser, O., Yogev, Y., Dolgin, V., Proskorovski-Ohayon, R., Perez, Y., Nudelman, H., Stoler, O., Rotblat, B., Lifschytz, T., Lotan, A., Meiri, G., Gitler, D., Birk, O. S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548587/ https://www.ncbi.nlm.nih.gov/pubmed/34702855 http://dx.doi.org/10.1038/s41467-021-26426-1 |
Ejemplares similares
-
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone
por: Yogev, Yuval, et al.
Publicado: (2023) -
IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma
por: Wormser, Ohad, et al.
Publicado: (2023) -
Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia
por: Balan, Shabeesh, et al.
Publicado: (2021) -
PSMC1
variant causes a novel neurological syndrome
por: Aharoni, Sarit, et al.
Publicado: (2022) -
A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13‐q21.3
por: Halperin, Daniel, et al.
Publicado: (2022)