tuberous sclerosis complex (tsc) is a genetic disorder that causes tumors to form in vital organs, primarily the brain, eyes, heart, kidneys, liver, lung and skin.
结节性硬化癥(tsc)是一种遗传病,可导致脑、眼睛、心脏、肾脏、肝脏和皮肤等重要器官发生肿瘤。
tuberous sclerosis complex (tsc) is a genetic disorder that causes tumors to form in vital organs, primarily the brain, eyes, heart, kidneys, liver, lung and skin.
结节性硬化癥是一种遗传病,可导致脑、眼睛、心脏、肾脏、肝脏、肺和皮肤等重要器官发生肿瘤。
abstract:objective to analyze the mutation of tsc gene in two sporadic patients with tuberous sclerosis complex (tsc).
摘要:目的 检测两例中国汉族结节性硬化癥散发病例的基因突变位点。