Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases

Publisher： John Wiley & Sons Inc

E-ISSN： 1528-1167|56|12|1931-1940

ISSN： 0013-9580

Source： EPILEPSIA, Vol.56, Iss.12, 2015-12, pp. : 1931-1940

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

De novo KCNT1 mutations in early‐onset epileptic encephalopathy

By  

EPILEPSIA, Vol. 56, Iss. 9, 2015-09 ,pp. : e121-e128

John Wiley & Sons Inc

Access to resources Recommend Favorite

Early onset epileptic encephalopathy caused by de novo SCN8A mutations

By  

EPILEPSIA, Vol. 55, Iss. 7, 2014-07 ,pp. : 994-1000

John Wiley & Sons Inc

Access to resources Recommend Favorite

The Surface Molecular Signature of Leukemic Cells Is Associated with NPM1 Mutations and FLT3-ITD in Patients with de novo Acute Myeloid Leukemia

By  

Acta Haematologica, Vol. 131, Iss. 3, 2013-10 ,pp. : 148-152

Karger

Access to resources Recommend Favorite

Mutations de novo de SYNGAP1 associées à la déficience intellectuelle non syndromique

By Hamdan Fadi F.   Gauthier Julie   Rouleau Guy A.   Michaud Jacques L.  

Médecine/sciences, Vol. 26, Iss. 2, 2011-01 ,pp. : 133-135

Edp Sciences

Access to resources Recommend Favorite

Otomycosis in immunocompetent patients: Clinical and mycological features. Our experience with 40 cases

By  

CLINICAL OTOLARYNGOLOGY, Vol. 43, Iss. 1, 2018-02 ,pp. : 373-377

John Wiley & Sons Inc

Access to resources Recommend Favorite