CADASIL,ageneticdisorderduetomutationsintheNOTCH3gene,ischaracterizedbymigrainewithaura,mooddisorders,recurrenttransientischemicattacks ...
CADASIL, a genetic disorder due to mutations in the NOTCH3 gene, is characterized by migraine with aura, mood disorders, recurrent transient ischemic attacks ...
cadasil中文CADASILcadasil醫學CADASIL radiologyCADASIL treatmentCADASIL MRICerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyCADASIL diagnostic criteriacadasil中文cadasil醫學cadasil與notch3基因突變在台灣群眾中的特性CADASIL MRIcadasil基因檢測CADASIL radiologynotch3基因檢測費用CADASIL syndromeCARASIL MRICADASIL treatmentCADASIL symptomsCOL4A1 MRICADASILCADASIL diagnosiscadasil全名CADASIL ICD-10CADASIL NOTCH3
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