Genetics of cerebellar disorders.

Valente, Enza Maria; Nuovo, Sara; Doherty, Dan

Valente, Enza Maria; Nuovo, Sara; Doherty, Dan.

Afiliación

Valente EM; Neurogenetics Unit, IRCCS Santa Lucia Foundation, Rome, Italy; Department of Molecular Medicine, University of Pavia, Pavia, Italy. Electronic address: enzamaria.valente@unipv.it.
Nuovo S; Neurogenetics Unit, IRCCS Santa Lucia Foundation, Rome, Italy; Department of Medicine and Surgery, University of Salerno, Salerno, Italy.
Doherty D; Department of Pediatrics, University of Washington and Seattle Children's Research Institute, Seattle, WA, United States.

Handb Clin Neurol ; 154: 267-286, 2018.

Article en En | MEDLINE | ID: mdl-29903444

Asunto(s)

Enfermedades Cerebelosas/genética; Pruebas Genéticas; Mutación/genética; Humanos

Palabras clave

DNA sequencing; ataxia; brain malformation; cerebellum; diagnostic approach; genetic; inheritance; testing

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cerebelosas / Pruebas Genéticas / Mutación Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Handb Clin Neurol Año: 2018 Tipo del documento: Article

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