A heterozygous missense variant in DLX3 leads to uterine leiomyomas and pregnancy losses in a consanguineous Iranian family-Reference-Cited by-同舟云学术

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A heterozygous missense variant in DLX3 leads to uterine leiomyomas and pregnancy losses in a consanguineous Iranian family

Published:2023-05 Issue: Volume:865 Page:147292
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Saboori-Darabi Samaneh,Carrera Paola,Akbari Arvand,Amiri-Yekta Amir,Almadani Navid,Battista Pipitone Giovanni,Shahrokh-Tehraninejad Ensieh,Lotfi Marzieh,Mazaheri Mahta,Totonchi Mehdi

Funder

Royan Institute

Shahid Sadoughi University of Medical Sciences

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference74 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods.,2010

2. Andrews, S., 2010. FastQC: a quality control tool for high throughput sequence data. Babraham Bioinformatics. https://www.bioinformatics.babraham.ac.uk/projects/fastqc/.

3. High cumulative incidence of uterine leiomyoma in black and white women: ultrasound evidence;Baird;Am. J. Obstet. Gynecol.,2003

4. Loss of DLX3 tumor suppressive function promotes progression of SCC through EGFR–ERBB2 pathway;Bajpai;Oncogene,2021

5. The Dlx3 protein harbors basic residues required for nuclear localization, transcriptional activity and binding to Msx1;Bryan;J. Cell Sci.,2000

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