Analysis of gene mutations and long-term follow-up in children with phenylalanine hydroxylase deficiency diagnosed by newborn screening

Q2 Medicine
Meng Sun, Yulin Li, Panpan Li, Gaijie Li, Yan Yan, Hui Zou
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引用次数: 0
通过新生儿筛查确诊的苯丙氨酸羟化酶缺乏症患儿的基因突变分析和长期随访
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
67
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