Mutation in ADORA1 identified as likely cause of early‐onset parkinsonism and cognitive dysfunction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 in ADORA1 identified as likely cause of early‐onset parkinsonism and cognitive dysfunction

Authors:	Elham Jaberi PhD Mohammad Rohani MD Gholam Ali Shahidi MD Shahriar Nafissi MD Ehsan Arefian PhD Masoud Soleimani PhD Abolfazl Moghadam MS Mohsen Karimi Arzenani PhD Farid Keramatian MS Brandy Klotzle PhD Jian‐Bing Fan PhD Casey Turk PhD Frank Steemers PhD Elahe Elahi PhD

Affiliation:	1. School of Biology, College of Science, University of Tehran, Tehran, Iran;2. Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran;3. Department of Neurology, Tehran University of Medical Sciences, Tehran, Iran;4. School of Medical Sciences, Tarbiat Modares University, Tehran, Iran;5. Center for Molecular Medicine, Karolinska Hospital, Stockholm, Sweden;6. Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran;7. Illumina, San Diego, California, USA

Abstract:

Keywords:	ADORA1 parkinsonism cognitive dysfunction dopamine receptor D1 exome sequencing