Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene

• We describe atypical features in a high percentage of the patients with BFIS. • We suggest to perform a long-term follow-up in patients without a benign outcome. • We also extend the mutational spectrum of PRRT2.

Gespeichert in:
Autor*in:

Guerrero-López, Rosa [verfasserIn]

Ortega-Moreno, Laura

Giráldez, Beatriz G.

Alarcón-Morcillo, Cristina

Sánchez-Martín, Gema

Nieto-Barrera, Manuel

Gutiérrez-Delicado, Eva

Gómez-Garre, Pilar

Martínez-Bermejo, Antonio

García-Peñas, Juan J.

Serratosa, José M.

Format:

E-Artikel

Sprache:

Englisch

Erschienen:

2014

Schlagwörter:

Learning difficulties

Epilepsy

Genetics

Infantile convulsions

Umfang:

5

Übergeordnetes Werk:

Enthalten in: Identification and measurement of gaps within sugarcane rows for site-specific management: Comparing different sensor-based approaches - Maldaner, Leonardo F. ELSEVIER, 2021, Amsterdam [u.a.]

Übergeordnetes Werk:

volume:108 ; year:2014 ; number:8 ; pages:1274-1278 ; extent:5

Links:

Volltext

DOI / URN:

10.1016/j.eplepsyres.2014.06.011

Katalog-ID:

ELV022846735

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