Expanding the Phenotypic Spectrum of CACNA1H Mutations.

Chourasia, Nitish; Ossó-Rivera, Henry; Ghosh, Ankita; Von Allmen, Gretchen; Koenig, Mary Kay

Chourasia, Nitish; Ossó-Rivera, Henry; Ghosh, Ankita; Von Allmen, Gretchen; Koenig, Mary Kay.

Afiliación

Chourasia N; McGovern Medical School, UTHealth, Division of Child and Adolescent Neurology, Houston, Texas. Electronic address: nitishchourasia@gmail.com.
Ossó-Rivera H; McGovern Medical School, UTHealth, Division of Child and Adolescent Neurology, Houston, Texas.
Ghosh A; McGovern Medical School, UTHealth, Division of Child and Adolescent Neurology, Houston, Texas.
Von Allmen G; McGovern Medical School, UTHealth, Division of Pediatric Epilepsy, Houston, Texas.
Koenig MK; McGovern Medical School, UTHealth, Mitochondrial Center of Excellence, Houston, Texas.

Pediatr Neurol ; 93: 50-55, 2019 04.

Article en En | MEDLINE | ID: mdl-30686625

Asunto(s)

Canales de Calcio Tipo T/genética; Epilepsia/genética; Epilepsia/fisiopatología; Adolescente; Niño; Preescolar; Epilepsias Parciales/genética; Epilepsias Parciales/fisiopatología; Femenino; Humanos; Lactante; Masculino; Mutación; Fenotipo

Palabras clave

CACNA1H; Focal epilepsy; Genetic epilepsy; Immunodeficiency; Multifocal epilepsy

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Canales de Calcio Tipo T / Epilepsia Tipo de estudio: Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2019 Tipo del documento: Article

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