A Novel Homozygous PDE 10A Variant Leading to Infantile-Onset Hyperkinesia.

Trieschmann, Gesa; Wach, Katharina; Abel, Maria; Tilgner, Eva; Berweck, Steffen; Zech, Michael

Trieschmann, Gesa; Wach, Katharina; Abel, Maria; Tilgner, Eva; Berweck, Steffen; Zech, Michael.

Afiliação

Trieschmann G; Specialist Centre for Paediatric Neurology, Neurorehabilitation and Epileptology, Schoen Clinic Vogtareuth, Vogtareuth, Bayern, Germany.
Wach K; Specialist Centre for Paediatric Neurology, Neurorehabilitation and Epileptology, Schoen Clinic Vogtareuth, Vogtareuth, Bayern, Germany.
Abel M; Department of Paediatrics, University Hospital Goettingen, Goettingen, Germany.
Tilgner E; Specialist Centre for Neurosurgery and Epilepsy Surgery, Vogtareuth, Bayern, Germany.
Berweck S; Social Paediatric Centre, DONAUISAR Klinikum Deggendorf, Deggendorf, Germany.
Zech M; Specialist Centre for Paediatric Neurology, Neurorehabilitation and Epileptology, Schoen Clinic Vogtareuth, Vogtareuth, Bayern, Germany.

Neuropediatrics ; 53(5): 386-387, 2022 10.

Article em En | MEDLINE | ID: mdl-35790203

Assuntos

Hipercinese; Homozigoto; Humanos; Mutação

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipercinese Limite: Humans Idioma: En Revista: Neuropediatrics Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Alemanha

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