Association Study of the 2-bp Deletion Polymorphism in Exon 6 of the CHRFAM7A Gene with Idiopathic Generalized Epilepsy

There is evidence of linkage between the 15q13–q14 locus, containing the gene encoding the α7 subunit (CHRNA7) of the neuronal nicotinic acetylcholine receptor (nAChR) and its partially duplicated isoform (CHRFAM7A), and epilepsy. Additionally, a 2-bp deletion polymorphism (c.497–498delTG; rs6715867...

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Detalhes bibliográficos
Main Authors: Rozycka, Agata, Dorszewska, Jolanta, Steinborn, Barbara, Lianeri, Margarita, Winczewska-Wiktor, Anna, Sniezawska, Aleksandra, Wisniewska, Kamila, Jagodzinski, Pawel P.
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2013
Assuntos:
Molecular Mechanisms of Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3806399/
https://ncbi.nlm.nih.gov/pubmed/24024466
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/dna.2012.1880
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