Cargando…
The association between the CCDC88A gene polymorphism at rs1437396 and alcohol use disorder, with or without major depression disorder
Girdin is a protein involved in neuronal migration and hippocampal development. It is encoded by the coiled-coil domain-containing 88A (CCDC88A) gene, located on the short arm of chromosome 2 (2p). The CCDC88A gene is modulated by the intergenic single-nucleotide polymorphism (SNP) of the rs1437396,...
Autores principales: | Bonea, Maria, Coroama, Constantin-Ionut, Popp, Radu Anghel, Miclutia, Ioana Valentina |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sciendo
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291494/ https://www.ncbi.nlm.nih.gov/pubmed/37357876 http://dx.doi.org/10.2478/aiht-2023-74-3690 |
Ejemplares similares
-
CCDC88B is required for pathogenesis of inflammatory bowel disease
por: Fodil, Nassima, et al.
Publicado: (2017) -
CCDC88A mutations cause PEHO-like syndrome in humans and mouse
por: Nahorski, Michael S., et al.
Publicado: (2016) -
Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants
por: Marguet, Florent, et al.
Publicado: (2021) -
Mutations in CCDC39 and CCDC40 are a major cause of primary ciliary dyskinesia with microtubule disorganisation
por: Antony, D, et al.
Publicado: (2012) -
Prognostic Relevance of CCDC88C (Daple) Transcripts in the Peripheral Blood of Patients with Cutaneous Melanoma
por: Dunkel, Ying, et al.
Publicado: (2018)