Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome - Concepedia

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Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome

DOI Full Paper Access

71

Citations

18

References

2014

Year

Mateusz Kolanczyk, Peter Krawitz, Jochen Hecht, Anna Hupalowska, Marta Miączyńska, Katrin Marschner, Claire Schlack, Denise Emmerich, Karolina Kobus, Uwe Kornak,

European Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsPathologyRitscher-schinzel/3c SyndromeMedicineMissense VariantNeurogeneticsDevelopmental Delay

References

	Year	Citations

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