Kerith-Rae Dias
3PUBLICATIONS
91CO-AUTHORS
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Publications (3)
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|Jul 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.Yuyang Chen, Ruebena Dawes, Hyung Chul Kim
|Apr 22, 2024
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.Yuyang Chen, Ruebena Dawes, Hyung Chul Kim
|Nov 17, 2020
Germline AGO2 mutations impair RNA interference and human neurological development.Davor Lessel, Daniela M Zeitler, Margot R F Reijnders
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