[Updated on Apr. 18] Integration of CiNii Articles into CiNii Research

A functional null mutation of SCN1B in a patient with Dravet syndrome.

Bibliographic Information

Title
A functional null mutation of SCN1B in a patient with Dravet syndrome.
Author
Patino G.A., Claes L.R., Lopez-Santiago L.F., Slat E.A., Dondeti R.S., Chen C., O'Malley H.A., Gray C.B., Miyazaki H., Nukina N., Oyama F., De Jonghe P., Isom L.L.

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Details

  • CRID
    1010000782039528321
  • Article Type
    journal article
  • Data Source
    • KAKEN

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