<scp>Bi‐allelic</scp> null variant in matrix metalloproteinase‐15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive-Reference-Cited by-同舟云学术

Bi‐allelic null variant in matrix metalloproteinase‐15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive

Published:2022-01-08 Issue:4 Volume:101 Page:403-410
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Abdelrahman Hanadi A.¹,Akawi Nadia¹,Al‐Shamsi Aisha M.²^ORCID,Ali Amanat¹,Al‐Jasmi Fatma¹³^ORCID,John Anne¹,Hertecant Jozef²,Al‐Gazali Lihadh³^ORCID,Ali Bassam R.¹⁴^ORCID

Affiliation:

1. Department of Genetics and Genomics, College of Medicine and Heath Sciences United Arab Emirates University Al‐Ain United Arab Emirates

2. Paediatrics Department Tawam hospital Al‐Ain United Arab Emirates

3. Department of Paediatrics, College of Medicine and Heath Sciences United Arab Emirates University Al‐Ain United Arab Emirates

4. Zayed Center for Health sciences United Arab Emirates University Al‐Ain United Arab Emirates

Funder

United Arab Emirates University

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14107

Reference29 articles.

1. Challenges in Matrix Metalloproteinases Inhibition

2. Biochemical and Biological Attributes of Matrix Metalloproteinases

3. Next generation matrix metalloproteinase inhibitors — Novel strategies bring new prospects

4. Matrix Metalloproteases as Influencers of the Cells’ Social Media

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