Further evidence of a causal association between AGO1, a critical regulator of microRNA formation, and intellectual disability/autism spectrum disorder-Reference-Cited by-同舟云学术

Further evidence of a causal association between AGO1, a critical regulator of microRNA formation, and intellectual disability/autism spectrum disorder

Published:2019-06 Issue:6 Volume:62 Page:103537
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Sakaguchi Asami,Yamashita Yukio,Ishii Tomohiro^ORCID,Uehara Tomoko^ORCID,Kosaki Kenjiro^ORCID,Takahashi Takao,Takenouchi Toshiki

Funder

Ministry of Health, Labour and Welfare, Japan

Japan Agency for Medical Research and Development

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference18 articles.

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4. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice;Keller;Nat. Genet.,2013

5. Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export;Legati;Nat. Genet.,2015

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1. Maintenance of Heterochromatin links Chromatin Modifiers and Neurodevelopment in Autism Spectrum Disorder;2023-10-10

2. A novel heterozygous truncating variant in the AGO1 gene in an Iranian family with schizophrenia as an unreported symptom;Annals of Human Genetics;2023-08-17

3. Identification of atlastin genetic modifiers in a model of hereditary spastic paraplegia in Drosophila;Human Genetics;2023-06-27

4. Complex congenital cardiovascular anomaly in a patient with AGO1 ‐associated disorder;American Journal of Medical Genetics Part A;2022-12-23

5. Decoding microRNAs in autism spectrum disorder;Molecular Therapy - Nucleic Acids;2022-12