An Update on the Phenotype, Genotype and Neurobiology of ADCY5-Related Disease.

Ferrini, Arianna; Steel, Dora; Barwick, Katy; Kurian, Manju A

Ferrini, Arianna; Steel, Dora; Barwick, Katy; Kurian, Manju A.

Afiliación

Ferrini A; Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, Zayed Centre for Research into Rare Disease in Children, London, United Kingdom.
Steel D; Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, Zayed Centre for Research into Rare Disease in Children, London, United Kingdom.
Barwick K; Department of Neurology, Great Ormond Street Hospital, London, United Kingdom.
Kurian MA; Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, Zayed Centre for Research into Rare Disease in Children, London, United Kingdom.

Mov Disord ; 36(5): 1104-1114, 2021 05.

Article en En | MEDLINE | ID: mdl-33934385

Asunto(s)

Discinesias; Trastornos Distónicos; Trastornos del Movimiento; Adenilil Ciclasas/genética; Trastornos Distónicos/genética; Genotipo; Humanos; Fenotipo

Palabras clave

ADCY5; dyskinesia; hyperkinesia; movement disorder; precision medicine

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos Distónicos / Discinesias / Trastornos del Movimiento Límite: Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

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