De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway - Concepedia

Concepedia

Publication | Open Access

De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway

DOI Full Paper Access

20

Citations

61

References

2022

Year

Maria Asif, Emrah Kaygusuz, Marwan Shinawi, Anna Nickelsen, Tzung‐Chien Hsieh, Prerana Wagle, Birgit Budde, Jennifer Hochscherf, Uzma Abdullah, Stefan Höning,

Human Genetics and Genomics Advances

References

	Year	Citations

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