RANBP2 Mutation in Clinically Undiagnosed Acute Necrotizing Encephalopathy

Indian J Pediatr. 2018 Sep;85(9):820-821. doi: 10.1007/s12098-018-2678-0. Epub 2018 Apr 24.

Authors

Sedat Işıkay^{1

2}, Yavuz Şahin³

Affiliations

¹ Department of Physiotherapy and Rehabilitation, School of Health Sciences, Hasan Kalyoncu University, Gaziantep, Turkey. [email protected].
² Department of Pediatric Neurology, Medical Park Hospital, 52063 Street, Şehitkamil, Gaziantep, Turkey. [email protected].
³ Department of Medical Genetics, Necip Fazıl City Hospital, Kahramanmaras, Turkey.

PMID: 29687329
DOI: 10.1007/s12098-018-2678-0

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Humans
Leukoencephalitis, Acute Hemorrhagic / diagnosis
Leukoencephalitis, Acute Hemorrhagic / genetics*
Molecular Chaperones / genetics*
Mutation*
Nuclear Pore Complex Proteins / genetics*

Substances

Molecular Chaperones
Nuclear Pore Complex Proteins
ran-binding protein 2