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Case Report: Reinterpretation and Reclassification of ARSB:p.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the CDH23 Gene

Overview of attention for article published in Frontiers in Pediatrics, February 2022
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Title
Case Report: Reinterpretation and Reclassification of ARSB:p.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the CDH23 Gene
Published in
Frontiers in Pediatrics, February 2022
DOI 10.3389/fped.2021.803732
Pubmed ID
Authors

Nahid Al Dhahouri, Amanat Ali, Jozef Hertecant, Fatma Al-Jasmi

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 2 33%
Researcher 1 17%
Unknown 3 50%
Readers by discipline Count As %
Medicine and Dentistry 2 33%
Neuroscience 1 17%
Unknown 3 50%