PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly

10.1126/sciadv.aax9852

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Bibliographic Details
Main Authors: Mzoughi, S., Di Tullio, F., Low, D.H.P., Motofeanu, C.-M., Ong, S.L.M., Wollmann, H., Wun, C.M., Kruszka, P., Muenke, M., Hildebrandt, F., Dunn, N.R., Messerschmidt, D.M., Guccione, E.
Other Authors: BIOCHEMISTRY
Format: Article
Published: American Association for the Advancement of Science 2021
Online Access:https://scholarbank.nus.edu.sg/handle/10635/198952
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Institution: National University of Singapore