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Article

Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.

Seizure - 1 Jan 2016

Cen Zhi-dong, Xie Fei, Xiao Jian-feng, Luo Wei

Abstract excerpt

Familial cortical myoclonic tremor with epilepsy (FCMTE) is an autosomal dominant epilepsy syndrome with considerable clinical and genetic heterogeneity. The most important clinical manifestations include adult onset, cortical myoclonic tremor, with or without epileptic seizures. Of the four loci reported, which included 8q24 (FCMTE1), 2p11.1-q12.2 (FCMTE2), 5p15.31-p15.1 (FCMTE3), and 3q26.32-3q28 (FCMTE4), only...

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PMID: 26751243
DOI: 10.1016/j.seizure.2015.12.004

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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