New CACNA1A deletions are associated to migraine phenotypes.

Grieco, G S; Gagliardi, S; Ricca, I; Pansarasa, O; Neri, M; Gualandi, F; Nappi, G; Ferlini, A; Cereda, C

Grieco, G S; Gagliardi, S; Ricca, I; Pansarasa, O; Neri, M; Gualandi, F; Nappi, G; Ferlini, A; Cereda, C.

Afiliación

Grieco GS; IRCCS Mondino Foundation, Genomic and post-Genomic Center, Pavia, Italy.
Gagliardi S; IRCCS Mondino Foundation, Genomic and post-Genomic Center, Pavia, Italy. stella.gagliardi@mondino.it.
Ricca I; IRCCS Mondino Foundation, Genomic and post-Genomic Center, Pavia, Italy.
Pansarasa O; IRCCS Mondino Foundation, Genomic and post-Genomic Center, Pavia, Italy.
Neri M; Unit of Medical Genetics, S. Anna University-Hospital, Ferrara, Italy.
Gualandi F; Unit of Medical Genetics, S. Anna University-Hospital, Ferrara, Italy.
Nappi G; IRCCS Mondino Foundation, Headache Science Center, Pavia, Italy.
Ferlini A; Unit of Medical Genetics, S. Anna University-Hospital, Ferrara, Italy.
Cereda C; IRCCS Mondino Foundation, Genomic and post-Genomic Center, Pavia, Italy.

J Headache Pain ; 19(1): 75, 2018 Aug 30.

Article en En | MEDLINE | ID: mdl-30167989

Asunto(s)

Canales de Calcio/genética; Deleción Cromosómica; Trastornos Migrañosos/genética; Fenotipo; Adulto; Análisis Mutacional de ADN; Exones/genética; Femenino; Humanos; Masculino; Persona de Mediana Edad; Mutación Puntual; Análisis de Secuencia de ADN

Palabras clave

CACNA1A; De novo; Deletion; Migraine phenotypes

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Canales de Calcio / Deleción Cromosómica / Trastornos Migrañosos Tipo de estudio: Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Headache Pain Asunto de la revista: MEDICINA INTERNA / NEUROLOGIA / PSICOFISIOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Italia

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