De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features - Concepedia

Concepedia

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De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features

80

Citations

16

References

2016

Year

Volkan Okur, Megan T. Cho, Lindsay B. Henderson, Kyle Retterer, Michael Schneider, Shannon G. Sattler, Dmitriy Niyazov, Meron Azage, Sharon E. Smith, Jonathan Picker,

Neurodevelopmental DisordersDevelopmental AnomalyDevelopmental BiologyGenetic DisorderNeurodevelopmental AbnormalitiesGeneticsPsychiatric GeneticsNeuroscienceDysmorphic FeaturesAbnormal DevelopmentNeuropathologyMedicineSocial SciencesNeurogenetics

References

	Year	Citations

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