Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients-Reference-Cited by-同舟云学术

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Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients

Published:2022-02-17 Issue:4 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Mosallaei Meysam¹,Ehtesham Naeim¹,Beheshtian Maryam¹,Khoshbakht Shahrouz¹^ORCID,Davarnia Behzad²,Kahrizi Kimia¹^ORCID,Najmabadi Hossein¹³^ORCID

Affiliation:

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

2. Department of Genetic and Pathology Ardabil University of Medical Sciences Ardabil Iran

3. Kariminejad ‐ Najmabadi Pathology & Genetics Centre Tehran Iran

Funder

Iran National Science Foundation

National Institute for Medical Research Development

University of Social Welfare and Rehabilitation Sciences

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1894

Reference69 articles.

1. Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights

2. Contrasting Effects of IG20 and Its Splice Isoforms, MADD and DENN-SV, on Tumor Necrosis Factor α-induced Apoptosis and Activation of Caspase-8 and -3

3. IQSEC2 and X-linked syndromal intellectual disability

4. Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

5. Expanding the genetic heterogeneity of intellectual disability

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