CEP152 is a genome maintenance protein disrupted in Seckel syndrome

Overview of attention for article published in Nature Genetics, December 2010

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So far, Dimensions has found 199 publications that cite this research output.

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Novel Variants of CEP152 in a Case of Compound-Heterozygous Inheritance of Epilepsy

Article in Global Medical Genetics (January 2024)

Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalities

Article in EBioMedicine (December 2023)

Centriolar subdistal appendages promote double‐strand break repair through homologous recombination

Article in EMBO Reports (September 2023)

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