机译:GBA GBA P.TRP378GLY突变是一种可能的法国加拿大创始人突变,导致陶cher病和突触核苷酸疗法
Montreal Neurological InstituteMcGill UniversityMontréal Quebec Canada;
Department of Epidemiology Biostatistics and Occupational HealthMcGill UniversityMontréal Quebec;
Department of HematologyJewish General Hospital McGill UniversityMontréal Quebec Canada;
Axe neurosciences du CHU de QuébecUniversité LavalQuébec Canada;
Montreal Neurological InstituteMcGill UniversityMontréal Quebec Canada;
Faculty of MedicineMcGill UniversityMontréal Quebec Canada;
Montreal Neurological InstituteMcGill UniversityMontréal Quebec Canada;
McGill Parkinson Program and Neurodegenerative Diseases Group Montreal Neurological;
Department of Pharmacology &
TherapeuticsMcGill UniversityMontréal Quebec Canada;
Division of Neurology Department of MedicineUniversity of TorontoToronto Ontario Canada;
Department of NeurologyMcGill University Montreal General HospitalMontreal Québec Canada;
Axe neurosciences du CHU de QuébecUniversité LavalQuébec Canada;
Hematology/OncologyCentre Hospitalier Universitaire Sainte‐JustineMontréal Quebec Canada;
Department of HematologyJewish General Hospital McGill UniversityMontréal Quebec Canada;
Mark Freedman and Judy Jacobs Program for Gaucher DiseaseSinai Health System and University of;
Montreal Neurological InstituteMcGill UniversityMontréal Quebec Canada;
Gaucher disease; GBA; Parkinson disease; REM sleep behavior disorder;
机译:GBA GBA P.TRP378GLY突变是一种可能的法国加拿大创始人突变,导致陶cher病和突触核苷酸疗法
机译:来自GAUCHER病3患者化合物杂合子的诱导多能干细胞系(INSAI001-A)用于GBA1基因中的突变
机译:鉴定GBA基因突变在19巴基斯坦病原体病患者中
机译:Sarcomere蛋白质基因突变和遗传性心脏病:β-心肌肌苷重链突变导致心内膜肌肌瘤和心力衰竭
机译:扩展孟德尔突变预测模型,该模型可根据疾病家族史预测是否存在致病突变。
机译:韩国非神经病性Gaucher病的GBA P.G85E突变:创始人和神经保护作用
机译:韩国非神经病性Gaucher病的GBA P.G85E突变:创始人和神经保护作用