Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesis-Reference-Cited by-同舟云学术

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Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesis

Published:2018-10-05 Issue:11 Volume:176 Page:2466-2469
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Sakaguchi Yuri¹^ORCID,Uehara Tomoko¹^ORCID,Suzuki Hisato¹,Sakamoto Yoshiaki²,Fujiwara Mineko¹,Kosaki Kenjiro¹,Takenouchi Toshiki³^ORCID

Affiliation:

1. Center for Medical Genetics; Keio University School of Medicine; Tokyo Japan

2. Department of Plastic and Reconstructive Surgery; Keio University School of Medicine; Tokyo Japan

3. Department of Pediatrics; Keio University School of Medicine; Tokyo Japan

Funder

Japan Agency for Medical Research and Development

Ministry of Health, Labour and Welfare

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40354/fullpdf

Reference17 articles.

1. Diagnostic and Statistical Manual of Mental Disorders

2. Genotype phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: Cleft palate in SMS is associated with larger deletions;Andrieux;Journal of Medical Genetics,2007

3. Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse;Bi;Genome Research,2002

4. MeCP2: Only 100% will do;Chao;Nature Neuroscience,2012

5. Prevalence and architecture of de novo mutations in developmental disorders;Deciphering Developmental Disorders Study;Nature,2017

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2. The Role of Thyroid Hormone in the Regulation of Cerebellar Development;Endocrinology and Metabolism;2021-08-31

3. TBL1XR1 Ensures Balanced Neural Development Through NCOR Complex-Mediated Regulation of the MAPK Pathway;Frontiers in Cell and Developmental Biology;2021-02-23

4. MeCP2: The Genetic Driver of Rett Syndrome Epigenetics;Frontiers in Genetics;2021-01-21

5. Nuclear Receptor Coactivators (NCOAs) and Corepressors (NCORs) in the Brain;Endocrinology;2020-05-25

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