Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness

Overview of attention for article published in Frontiers in Genetics, December 2021

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New Research: Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness: Splice site mutations contribute to a significant portion of the genetic causes for mendelian disorders including deafness. By… https://t.co/W

08 Dec 2021

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