Related Experiment Video
Updated: Oct 9, 2025

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype
Aline Floch1,2,3, Sunitha Vege1, Philip Berardi4
1Immunohematology and Genomics Laboratory, New York Blood Center, New York, New York, USA.
Transfusion
|December 22, 2021
Abstract
No abstract available in PubMed .
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