Concepedia

Publication | Open Access

SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype

DOIFull Paper Access

77

Citations

58

References

2021

Year

Marialetizia Motta, Giulia Fasano, Sina Gredy, Julia Brinkmann, Adeline Bonnard, Pelin Özlem Şimşek‐Kiper, Elif Yılmaz Güleç, L. Essaddam, Gülen Eda Ütine, Ingrid G. Prandi,
The American Journal of Human Genetics

References

YearCitations

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