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Article

A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28

20 Jun 2012

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Share to Genetics and Neurodevelopmental Disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22713812
DOI: 10.1038/ejhg.2012.133

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28PMID 22713812Read ↗

Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.Semantic proximity Read ↗

Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.Semantic proximity Read ↗

A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy.Semantic proximity Read ↗

Familial benign nonprogressive myoclonic epilepsies.Semantic proximity Read ↗

Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus.Semantic proximity Read ↗

Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansionsSemantic proximity Read ↗

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families.Semantic proximity Read ↗

Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizuresSemantic proximity Read ↗

History of familial adult myoclonus epilepsy/benign adult familial myoclonic epilepsy around the world.Semantic proximity Read ↗

A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2.Semantic proximity Read ↗

Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion.Semantic proximity Read ↗

Absence of linkage to 8q23.3-q24.1 and 2p11.1-q12.2 in a new BAFME pedigree in China: indication of a third locus for BAFME.Semantic proximity Read ↗

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