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Assessment of children in the autistic spectrum disorder that carry the Thr92Ala-DIO2 polymorphism
Author(s) -
A. A. e Marcondes,
Thiago G. B. Gomez,
T.T. Ravache,
Alice Batistuzzo,
Fernanda Beraldo Lorena,
Cristiane Silvestre de Paula,
Rosane Lowenthal,
Antonio C. Bianco,
Miriam O. Ribeiro
Publication year - 2021
Publication title -
journal of endocrinological investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.034
H-Index - 84
eISSN - 1720-8386
pISSN - 0391-4097
DOI - 10.1007/s40618-020-01497-x
Subject(s) - minor allele frequency , autism spectrum disorder , autism , psychology , population , wechsler adult intelligence scale , genotype , clinical psychology , psychiatry , pediatrics , allele frequency , medicine , cognition , genetics , biology , environmental health , gene
A polymorphism in the type 2 deiodinase (Thr92Ala-DIO2) gene has been associated with behavioral and cognitive dysfunction as well as neurodegeneration and oxidative stress in the central nervous system.

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