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

Sikora, Jakub; Jedlickova, Ivana; Pristoupilova, Anna; Stranecky, Viktor; Honzik, Tomas

Sikora, Jakub; Jedlickova, Ivana; Pristoupilova, Anna; Stranecky, Viktor; Honzik, Tomas.

Afiliação

Sikora J; 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.
Jedlickova I; Institute of Pathology, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
Pristoupilova A; 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.
Stranecky V; 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.
Honzik T; 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.

Ann Clin Transl Neurol ; 8(4): 994-1001, 2021 04.

Article em En | MEDLINE | ID: mdl-33780169

Assuntos

Heterogeneidade Genética; Doenças Neurodegenerativas; Humanos; Corpos de Inclusão Intranuclear; Doenças Neurodegenerativas/genética

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Heterogeneidade Genética / Doenças Neurodegenerativas Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google