New mutations in KCNT2 gene causing early infantile epileptic encephalopathy type 57: Case study and literature review

• Autorzy: Alagoz M. , Kherad N. , Bozkurt S. , Yuksel A.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Acta Biochimica Polonica
• Rocznik: 2020
• Tom: 67
• Numer: 3
• Opis fizyczny: p.431-434,fig.,ref.

Twórcy

autor

Alagoz M.

• Department of Molecular Biology and Genetics, Genome Centre, Biruni University, Zeytinburnu, Istanbul, Turkey

autor

Kherad N.

• Department of Molecular Biology and Genetics, Genome Centre, Biruni University, Zeytinburnu, Istanbul, Turkey

autor

Bozkurt S.

• Istinye University Faculty of Medicine, Maltepe, Zeytinburnu, Istanbul, Turkey

autor

Yuksel A.

• Department of Molecular Biology and Genetics, Genome Centre, Biruni University, Zeytinburnu, Istanbul, Turkey

Identyfikatory

DOI

10.18388/abp.2020_5364