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EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality

Crossref DOI link: https://doi.org/10.1038/gim.2016.86

Published Print: 2017-02

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Bailey, Julia N.

Patterson, Christopher

de Nijs, Laurence

Durón, Reyna M.

Nguyen, Viet-Huong

Tanaka, Miyabi

Medina, Marco T.

Jara-Prado, Aurelio

Martínez-Juárez, Iris E.

Ochoa, Adriana

Molina, Yolli

Suzuki, Toshimitsu

Alonso, María E.

Wight, Jenny E.

Lin, Yu-Chen

Guilhoto, Laura

Targas Yacubian, Elza Marcia

Machado-Salas, Jesús

Daga, Andrea

Yamakawa, Kazuhiro

Grisar, Thierry M.

Lakaye, Bernard

Delgado-Escueta, Antonio V.
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Text and Data Mining valid from 2017-02-01

Text and Data Mining valid from 2017-02-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2016.86

Content Type: article

Copyright: © 2017, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics