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Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease
University of Washington Center for Mendelian Genomics, Amlie Pinard, Wenlei Ye, Stuart M. Fraser, Jill A. Rosenfeld, Pavel Pichurin, Scott E. Hickey, Dongchuan Guo, Alana C. Cecchi, Maura L. Boerio, Stphanie Guey, Chaker Aloui, Kwanghyuk Lee, Markus Kraemer, Saleh Omar Alyemni, Michael J. Bamshad, Deborah A. Nickerson, Elisabeth Tournier-Lasserve, Shozeb Haider, Sheng Chih Jin
- Department of Genetics
- Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
- DBBS - Computational and Systems Biology
- DBBS - Human and Statistical Genetics
- DBBS - Molecular Genetics and Genomics
- DBBS - Neurosciences
- Institute of Clinical and Translational Sciences (ICTS)
- Center of Regenerative Medicine
- Hope Center for Neurological Disorders
- Intellectual and Developmental Disabilities Research Center (IDDRC)
- NeuroGenomics and Informatics Center
Research output: Contribution to journal › Article › peer-review
14
Scopus
citations