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Advanced filters: Author: Saadettin Kayipmaz Clear advanced filters

  • Bernd Wollnik and colleagues report mutations in CEP152 cause Seckel syndrome, which is characterized by short stature, severe microcephaly and mental retardation. The work suggests that CEP152 has a function in genome maintenance.

    • Ersan Kalay
    • Gökhan Yigit
    • Bernd Wollnik
    Research
    Nature Genetics
    Volume: 43, P: 23-26