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Fragile X Syndrome: From Molecular Aspect to Clinical Treatment.
Protic, Dragana D; Aishworiya, Ramkumar; Salcedo-Arellano, Maria Jimena; Tang, Si Jie; Milisavljevic, Jelena; Mitrovic, Filip; Hagerman, Randi J; Budimirovic, Dejan B.
Afiliação
  • Protic DD; Department of Pharmacology, Clinical Pharmacology and Toxicology, Faculty of Medicine, University of Belgrade, 11129 Belgrade, Serbia.
  • Aishworiya R; Medical Investigation of Neurodevelopmental Disorders (MIND) Institute UCDH, University of California Davis, 2825 50th Street, Sacramento, CA 95817, USA.
  • Salcedo-Arellano MJ; Khoo Teck Puat-National University Children's Medical Institute, National University Health System, 5 Lower Kent Ridge Road, Singapore 119074, Singapore.
  • Tang SJ; Medical Investigation of Neurodevelopmental Disorders (MIND) Institute UCDH, University of California Davis, 2825 50th Street, Sacramento, CA 95817, USA.
  • Milisavljevic J; Department of Pediatrics, University of California Davis School of Medicine, Sacramento, CA 95817, USA.
  • Mitrovic F; Department of Pathology and Laboratory Medicine, University of California Davis School of Medicine, Sacramento, CA 95817, USA.
  • Hagerman RJ; Medical Investigation of Neurodevelopmental Disorders (MIND) Institute UCDH, University of California Davis, 2825 50th Street, Sacramento, CA 95817, USA.
  • Budimirovic DB; Faculty of Medicine, University of Belgrade, 11129 Belgrade, Serbia.
Int J Mol Sci ; 23(4)2022 Feb 09.
Article em En | MEDLINE | ID: mdl-35216055

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil Tipo de estudo: Screening_studies Limite: Animals / Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil Tipo de estudo: Screening_studies Limite: Animals / Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2022 Tipo de documento: Article