| 标题 |
Mutations causing profound biotinidase deficiency in children ascertained by newborn screening in the United States occur at different frequencies than in symptomatic children |
| 网址 | |
| DOI | |
| 其它 |
期刊:Pediatric research 作者:Norrgard KJ; Pomponio RJ; Hymes J; Wolf B 出版日期:1999/07/01 |
| 求助人 | |
| 下载 | 求助已完成,仅限求助人下载。 |
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(2025-6-4)