Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5

E-ISSN： 2328-9503|2|5|575-580

ISSN： 2328-9503

Source： Annals Of Clinical And Translational Neurology, Vol.2, Iss.5, 2015-05, pp. : 575-580

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

Case report: vitamin D‐dependent rickets type 1 caused by a novel CYP27B1 mutation

Clinical Case Reports, Vol. 3, Iss. 12, 2015-12 ,pp. : 1012-1016

John Wiley & Sons Inc

Access to resources Recommend Favorite

Familial florid Cemento‐osseous dysplasia – case report and review of literature

Clinical Case Reports, Vol. 3, Iss. 12, 2015-12 ,pp. : 1034-1037

John Wiley & Sons Inc

Access to resources Recommend Favorite

Neuropathology of childhood‐onset basal ganglia degeneration caused by mutation of VAC14

Annals Of Clinical And Translational Neurology, Vol. 4, Iss. 12, 2017-12 ,pp. : 859-864

John Wiley & Sons Inc

Access to resources Recommend Favorite

Asystole, rhabdomyolysis and acute renal failure as initial presentation of phaeochromocytoma in multiple endocrine neoplasia (MEN) type IIA

By KÖPPEL C SCHIROP T BARCKOW D FREI U

Clinical Intensive Care, Vol. 6, Iss. 5, 1995-10 ,pp. : 245-245

Ashgate Publishing Ltd

Access to resources Recommend Favorite

Spontaneous remission in three cases of AML M5 with NPM1 mutation

Clinical Case Reports, Vol. 3, Iss. 11, 2015-11 ,pp. : 955-959

John Wiley & Sons Inc

Access to resources Recommend Favorite