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更正：生物素酶缺乏症：巴西患者的基因型-生化表型关联

Correction: Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients.

作者信息

Borsatto Taciane, Sperb-Ludwig Fernanda, Lima Samyra E, Carvalho Maria R S, Fonseca Pablo A S, Camelo José S, Ribeiro Erlane M, de Medeiros Paula F V, Lourenço Charles M, de Souza Carolina F M, Boy Raquel, Félix Têmis M, Bittar Camila M, Pinto Louise L C, Neto Eurico C, Blom Henk J, Schwartz Ida V D

出版信息

PLoS One. 2017 Jun 22;12(6):e0180463. doi: 10.1371/journal.pone.0180463. eCollection 2017.

DOI:10.1371/journal.pone.0180463
PMID:28640880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5481009/
Abstract

[This corrects the article DOI: 10.1371/journal.pone.0177503.].

摘要

[本文更正了文章的数字对象标识符：10.1371/journal.pone.0177503。]

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引用本文的文献

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Newborn Screening for Biotinidase Deficiency. The Experience of a Regional Center in Italy.新生儿生物素酶缺乏症筛查：意大利某地区中心的经验
Front Pediatr. 2021 May 31;9:661416. doi: 10.3389/fped.2021.661416. eCollection 2021.

本文引用的文献

1
Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients.生物素酶缺乏症：巴西患者的基因型-生化表型关联
PLoS One. 2017 May 12;12(5):e0177503. doi: 10.1371/journal.pone.0177503. eCollection 2017.