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pro vyhledávání: '"Arin Khadra"'
Autor:
Ernestine Saumweber, Slim Mzoughi, Arin Khadra, Anja Werberger, Sven Schumann, Ernesto Guccione, Michael J. Schmeisser, Susanne J. Kühl
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Mutations in PRDM15 lead to a syndromic form of holoprosencephaly (HPE) known as the Galloway–Mowat syndrome (GAMOS). While a connection between PRDM15, a zinc finger transcription factor, and WNT/PCP signaling has been established, there is a crit
Externí odkaz:
https://doaj.org/article/78d2540a478644248a459c33f482b656