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Comment on ‘p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small‐vessel occlusion in elderly Japanese males’
Authors:A. Satomura  M. Yanai  T. Fujita  T. Nakayama
Affiliation:1. Division of Laboratory Medicine, Department of Pathology and Microbiology, Nihon University School of Medicine, , Itabashi, Tokyo, Japan;2. Division of General Medicine, Department of Medicine, Nihon University School of Medicine, , Itabashi, Tokyo, Japan;3. Division of Nephrology, Hypertension and Endocrinology, Department of Medicine, Nihon University School of Medicine, , Itabashi, Tokyo, Japan
Abstract:
Keywords:E66Q mutation  Fabry disease
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