Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy

Authors:	Teresa Milano Simona Cappelletti Nicola Pietrafusa Enrico Silvio Bertini Federico Vigevano Nicola Specchio

Affiliation:	1. Department of Biochemical Science “Rossi Fanelli”, Sapienza University of Rome, Rome, Italy;2. Unit of Clinical Psychology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy;3. Division of Neurology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy;4. Department of Basic Medical Sciences, Neurosciences and Sense Organs, University of Bari, Bari, Italy;5. Unit of Molecular Medicine for Neuromuscular and Neurodegenerative Diseases, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy

Abstract:

Keywords:	Benign familial infantile epilepsies CHRNA2 gene Acetylcholine receptor Benign epilepsies Autosomal dominant nocturnal frontal lobe epilepsy