更正：唐纳利等人。新生儿筛查中检测出的一例苯丙氨酸羟化酶缺乏性高苯丙氨酸血症：早期检测的临床结果。2024年，[具体卷期]，7页。
Correction: Donnelly et al. A Case of -Deficient Hyperphenylalaninemia Detected on Newborn Screening: Clinical Outcomes from Early Detection. 2024, , 7.
作者信息
Donnelly Colleen, Estrella Lissette, Ginevic Ilona, Ganesh Jaya
机构信息
Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
出版信息
Int J Neonatal Screen. 2025 Apr 23;11(2):28. doi: 10.3390/ijns11020028.
Abstract
In the original publication [...].
摘要
在原始出版物中 [...]。
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Correction: Donnelly et al. A Case of -Deficient Hyperphenylalaninemia Detected on Newborn Screening: Clinical Outcomes from Early Detection. 2024, , 7.更正：唐纳利等人。新生儿筛查中检测出的一例苯丙氨酸羟化酶缺乏性高苯丙氨酸血症：早期检测的临床结果。2024年，[具体卷期]，7页。
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Correction: Furnier et al. Translating Molecular Technologies into Routine Newborn Screening Practice. . 2020, , 80.更正：弗尔尼耶等人。将分子技术转化为常规新生儿筛查实践。。2020年，，80。
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本文引用的文献
1
A Case of -Deficient Hyperphenylalaninemia Detected on Newborn Screening: Clinical Outcomes from Early Detection.新生儿筛查发现的一例苯丙氨酸羟化酶缺乏型高苯丙氨酸血症：早期检测的临床结果
Int J Neonatal Screen. 2024 Jan 17;10(1):7. doi: 10.3390/ijns10010007.
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