Genetic heterogeneity of neuronal intranuclear inclusion disease: What about the infantile variant?

Affiliations

Jakub Sikora: Research Unit for Rare Diseases Department of Paediatrics and Inherited Metabolic Disorders First Faculty of Medicine Charles University and General University Hospital Prague Czech Republic
Ivana Jedlickova: Research Unit for Rare Diseases Department of Paediatrics and Inherited Metabolic Disorders First Faculty of Medicine Charles University and General University Hospital Prague Czech Republic
Anna Pristoupilova: Research Unit for Rare Diseases Department of Paediatrics and Inherited Metabolic Disorders First Faculty of Medicine Charles University and General University Hospital Prague Czech Republic
Viktor Stranecky: Research Unit for Rare Diseases Department of Paediatrics and Inherited Metabolic Disorders First Faculty of Medicine Charles University and General University Hospital Prague Czech Republic
Tomas Honzik: Research Unit for Rare Diseases Department of Paediatrics and Inherited Metabolic Disorders First Faculty of Medicine Charles University and General University Hospital Prague Czech Republic

Abstract

No abstracts available.

ISSN: 2328-9503 (Online)
Publisher: Wiley
Country of publisher: United States
LCC subjects: Medicine: Internal medicine: Neurosciences. Biological psychiatry. Neuropsychiatry: Neurology. Diseases of the nervous system
Website: https://onlinelibrary.wiley.com/journal/23289503