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Truncating ASXL1 mutations in Bohring-Opitz Syndrome cause epigenetically driven upregulation of Wnt signaling

Document Type

Journal

Author

Lin, Isabella; Wei, Angela; Awamleh, Zain; Singh, Meghna; Ning, Aileen; Herrera, Analeyla; Russell, Bianca; Weksberg, Rosanna; Arboleda, Valerie

Source

EUROPEAN JOURNAL OF HUMAN GENETICS; JAN 2024, 32 p38-p39, 2p. Supplement: 1

Subject

Language

English

ISSN

14765438

Online Access

Web of Science JCR 저널정보 Find it@PNU

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