| 标题 |
A glycine250--> aspartate substitution in the alpha-subunit of hexosaminidase A causes juvenile-onset Tay-Sachs disease in a Lebanese-Canadian family |
| 网址 | |
| DOI | |
| 其它 |
期刊:Human mutation 作者:Trop I; Kaplan F; Brown C; Mahuran D; Hechtman P 出版日期:1992/01/01 |
| 求助人 | |
| 下载 |
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(2025-6-4)