Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment-Reference-Cited by-同舟云学术

Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment

Published:2021-08-23 Issue: Volume: Page:1-12
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Souissi Amal¹^ORCID,Abdelmalek Driss Dorra¹,Chakchouk Imen²,Ben Said Mariem¹,Ben Ayed Ikhlas¹³,Mosrati Mohamed Ali¹,Elloumi Ines¹,Tlili Abdelaziz⁴⁵,Aifa Sami¹,Masmoudi Saber¹

Affiliation:

1. Laboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia

2. Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX, USA

3. Medical Genetic Department, University Hedi Chaker Hospital of Sfax, Sfax, Tunisia

4. Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates

5. Human Genetics and Stem Cell Laboratory, Research Institute of Sciences and Engineering, University of Sharjah, Sharjah, United Arab Emirates

Publisher

Informa UK Limited

Subject

Molecular Biology,General Medicine,Structural Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/07391102.2021.1953600

Reference49 articles.

1. Alpha Helices Are More Robust to Mutations than Beta Strands

2. Phosphorylation of the Kinase Domain Regulates Autophosphorylation of Myosin IIIA and Its Translocation in Microvilli

3. A Millennial Myosin Census

4. Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss

5. Diagnostic Application of Targeted Resequencing for Familial Nonsyndromic Hearing Loss

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