A novel variant of C12orf4 linked to autosomal recessive intellectual disability type 66 with phenotype expansion-Reference-Cited by-同舟云学术

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A novel variant of C12orf4 linked to autosomal recessive intellectual disability type 66 with phenotype expansion

Published:2022-01-31 Issue: Volume: Page:
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:The Journal of Gene Medicine

Author:

Rashvand Zahra¹,Kahrizi Kimia²,Najmabadi Hossein²,Najafipour Reza²,Omrani Mir Davood¹

Affiliation:

1. Department of Medical Genetics Shahid Beheshti University of Medical Sciences Tehran Iran

2. Genetics Research Center University of Social Welfare and Rehabilitation Sciences Tehran Iran

Funder

Iran National Science Foundation

National Institute for Medical Research Development

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgm.3406

Reference26 articles.

1. Prevalence of intellectual disability: A meta-analysis of population-based studies

2. An anatomically comprehensive atlas of the adult human brain transcriptome

3. Deep sequencing reveals 50 novel genes for recessive cognitive disorders

4. Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

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