Mutations in sphingolipid metabolism genes are associated with ADHD

ABSTRACT: Attention deficit hyperactivity disorder (ADHD) is the most prevalent neurodevelopmental disorder in children, with genetic factors accounting for 75-80% of the phenotypic variance. Recent studies have suggested that ADHD patients might present with atypical central myelination that can pe...

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Autores:

Arcos Burgos, Oscar Mauricio
Palacio Ortiz, Juan David
Lopera Restrepo, Francisco Javier
Acosta, María T.
Martínez, Ariel F.
Vélez Vallbuena, Jorge Iván
Henriquez Henriquez, Marcela
Pineda Salazar, David Antonio
Quiroga, Teresa
Worgall, Tilla S.
Deckelbaum, Richard J.
Mastronardi, Claudio
Molina, Brooke S. G.
Muenke, Maximilian

Tipo de recurso:

Article of investigation

Fecha de publicación:

2020

Institución:

Universidad de Antioquia

Repositorio:

Repositorio UdeA

Idioma:

eng

OAI Identifier:

oai:bibliotecadigital.udea.edu.co:10495/42124

Acceso en línea:

https://hdl.handle.net/10495/42124

Palabra clave:

Attention Deficit Disorder with Hyperactivity
Trastorno por Déficit de Atención con Hiperactividad
Genetic Predisposition to Disease
Predisposición Genética a la Enfermedad
Mutation
Mutación
Polymorphism, Single Nucleotide
Polimorfismo de Nucleótido Simple
Sphingolipids
Esfingolípidos
Sphingomyelin Phosphodiesterase
Esfingomielina Fosfodiesterasa
https://id.nlm.nih.gov/mesh/D001289
https://id.nlm.nih.gov/mesh/D020022
https://id.nlm.nih.gov/mesh/D009154
https://id.nlm.nih.gov/mesh/D020641
https://id.nlm.nih.gov/mesh/D013107
https://id.nlm.nih.gov/mesh/D013108

Rights

openAccess

License

http://creativecommons.org/licenses/by/2.5/co/