Loss of Function Variant in <i>SMAD6</i> Is Associated With a Novel Phenotype of Internal Carotid Artery Dissection-Reference-Cited by-同舟云学术

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Loss of Function Variant in SMAD6 Is Associated With a Novel Phenotype of Internal Carotid Artery Dissection

Published:2024-08 Issue:4 Volume:17 Page:
ISSN:2574-8300
Container-title:Circulation: Genomic and Precision Medicine
language:en
Short-container-title:Circ: Genomic and Precision Medicine

Author:

Alghamdi Malak A.¹^ORCID,Alqarawi Wael²^ORCID,Alharbi Essa³^ORCID,Balahmar Reham M.³^ORCID,Alruqi Haya³^ORCID,Jadu Nisserin⁴^ORCID,Alhomidan Majid⁵^ORCID,Alghamdi Mohammed Hussien²^ORCID,Almontashiri Naif A.M.³⁶^ORCID

Affiliation:

1. Pediatric Department (M.A.A.)

2. Department of Cardiac Sciences (W.A., M.H.A.)

3. Center for Genetics and Inherited Diseases (E.A., R.M.B., H.A., N.A.M.A.)

4. College of Medicine Research Centre (N.J.)

5. Radiology Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia (M.A.).

6. Faculty of Applied Medical Sciences (N.A.M.A.), Taibah University, Almadinah Almunwarah, Saudi Arabia.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference5 articles.

1. A role for Smad6 in development and homeostasis of the cardiovascular system

2. SMAD6-deficiency in human genetic disorders

3. A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy

4. Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden

5. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

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