Reply: De novo mutations in CLDN5: alternating hemiplegia of childhood or not?

Desguerre, Isabelle; Aubart, Melodie; Hashimoto, Yosuke; Poirier, Karine; Kaminska, Anna; Alison, Marianne; Boddaert, Nathalie; Munnich, Arnold; Campbell, Matthew

Desguerre, Isabelle; Aubart, Melodie; Hashimoto, Yosuke; Poirier, Karine; Kaminska, Anna; Alison, Marianne; Boddaert, Nathalie; Munnich, Arnold; Campbell, Matthew.

Afiliação

Desguerre I; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Aubart M; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Hashimoto Y; Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.
Poirier K; INSERM UMR1163, Institut Imagine, Paris University, Paris 75015, France.
Kaminska A; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Alison M; Department of Pediatric Radiology, Hospital Robert Debré, Université Paris Cité, Paris F-75015, France.
Boddaert N; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Munnich A; INSERM UMR1163, Institut Imagine, Paris University, Paris 75015, France.
Campbell M; Department of Pediatric Radiology, Hospital Necker Enfants Malades, Université Paris Cité, Paris F-75015, France.

Brain ; 146(8): e59-e60, 2023 08 01.

Article em En | MEDLINE | ID: mdl-36825462

Assuntos

Hemiplegia; Humanos; Hemiplegia/genética; Mutação/genética; Claudina-5/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemiplegia Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França

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