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Tay–Sachs disease - Wikipedia, the free encyclopedia
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日期：2024-05-27
Tay–Sachs disease (also known as GM2 gangliosidosis or hexosaminidase A deficiency ) is a rare autosomal recessive genetic disorder. In its most common variant (known as infantile Tay–Sachs disease), it causes a progressive deterioration of nerve cells an...看更多
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