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

• 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.
• 其他作者: BIOCHEMISTRY
• 格式: Article
• 出版: American Association for the Advancement of Science 2021
• 在線閱讀: https://scholarbank.nus.edu.sg/handle/10635/198952

10.1126/sciadv.aax9852