Protein phenotype diagnosis of autosomal dominant calmodulin mutations causing irregular heart rhythms-Reference-Cited by-同舟云学术

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Protein phenotype diagnosis of autosomal dominant calmodulin mutations causing irregular heart rhythms

Published:2018-06-22 Issue:10 Volume:119 Page:8233-8248
ISSN:0730-2312
Container-title:Journal of Cellular Biochemistry
language:en
Short-container-title:J. Cell. Biochem.

Author:

Shaik Noor A.¹²^ORCID,Awan Zuhier A.³,Verma Prashant K.¹,Elango Ramu¹²,Banaganapalli Babajan¹²^ORCID

Affiliation:

1. Department of Genetic Medicine, Faculty of MedicineKing Abdulaziz UniversityJeddahSaudi Arabia

2. Princess Al‐Jawhara Al‐Brahim Centre of Excellence in Research of Hereditary Disorders (PACER‐HD)King Abdulaziz UniversityJeddahSaudi Arabia

3. Department of Clinical Biochemistry, Faculty of MedicineKing Abdulaziz UniversityJeddahSaudi Arabia

Funder

Deanship of Scientific Research, King Abdulaziz University

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcb.26834

Reference65 articles.

1. Calmodulin supports both inactivation and facilitation of L-type calcium channels

2. Arrhythmogenic Calmodulin Mutations Disrupt Intracellular Cardiomyocyte Ca 2+ Regulation by Distinct Mechanisms

3. Localization of the Human Bona Fide Calmodulin Genes CALM1, CALM2, and CALM3 to Chromosomes 14q24-q31, 2p21.1-p21.3, and 19q13.2-q13.3

4. Multiple divergent mRNAs code for a single human calmodulin.

5. Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

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