Reply: IREB2-associated neurodegeneration.

Maio, Nunziata; Ghosh, Manik C; Costain, Gregory; Carnevale, Amanda; Si, Yue; Yoon, Grace; Rouault, Tracey A

Maio, Nunziata; Ghosh, Manik C; Costain, Gregory; Carnevale, Amanda; Si, Yue; Yoon, Grace; Rouault, Tracey A.

Afiliação

Maio N; Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD, USA.
Ghosh MC; Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD, USA.
Costain G; Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Carnevale A; Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Si Y; GeneDx, Gaithersburg, MD, USA.
Yoon G; Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Rouault TA; Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Brain ; 142(8): e41, 2019 08 01.

Article em En | MEDLINE | ID: mdl-31243430

Assuntos

Predisposição Genética para Doença; Polimorfismo de Nucleotídeo Único; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

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