SCIENTIFIC HUB

Follow the evidence.

107.521 articles found

Source record

Epileptic encephalopathy with features of rapid-onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation.

Tran L, Richards J, McDonald M, McConkie-Rosell A, Stong N, Jasien J, Shashi V, Mikati MA.

Epileptic Disord · 2020-02-01

DOI: 10.1684/epd.2020.1127PMID: 32043468

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

Filters

Filters

Clear
Publication year
Research area
Author
Journal
Publication type
Source & language
Open accessAccess does not establish reuse rights.