《首例导致生物素酶缺乏症的连续基因缺失：三名斯里兰卡儿童的酶缺乏症》[《分子遗传学与代谢报告》2 (2016) 81 - 84]勘误
Corrigendum to "First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children" [Mol. Genet. Metab. Rep. 2 (2016) 81-84].
作者信息
Senanayake Danika Nadeen, Jasinge Eresha A, Pindolia Kirit, Wanigasinghe Jithangi, Monaghan Kristin, Suchy Sharon F, Wei Sainan, Jaysena Subashini, Wolf Barry
机构信息
Department of Chemical Pathology, North Columbo Teaching Hospital, Columbo, Sri Lanka.
Chemical Pathology, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka.
出版信息
Mol Genet Metab Rep. 2016 Apr 12;11:95. doi: 10.1016/j.ymgmr.2016.04.001. eCollection 2017 Jun.
Abstract
[This corrects the article DOI: 10.1016/j.ymgmr.2015.01.005.].
摘要
[本文更正了文章的数字对象标识符：10.1016/j.ymgmr.2015.01.005。]
相似文献
1
Corrigendum to "First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children" [Mol. Genet. Metab. Rep. 2 (2016) 81-84].《首例导致生物素酶缺乏症的连续基因缺失：三名斯里兰卡儿童的酶缺乏症》[《分子遗传学与代谢报告》2 (2016) 81 - 84]勘误
Mol Genet Metab Rep. 2016 Apr 12;11:95. doi: 10.1016/j.ymgmr.2016.04.001. eCollection 2017 Jun.
2
First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children.首例导致生物素酶缺乏症的连续性基因缺失：三名斯里兰卡儿童的酶缺乏症
Mol Genet Metab Rep. 2015 Feb 7;2:81-84. doi: 10.1016/j.ymgmr.2015.01.005. eCollection 2015 Mar.
4
Corrigendum to "Digenic variants of planar cell polarity genes in human neural tube defect patients." Mol Genet Metab. 2018 May;124(1):94-100. doi:10.1016/j.ymgme.2018.03.005. Epub 2018 Mar 18. https://pubmed.ncbi.nlm.nih.gov/29573971/.《人类神经管缺陷患者平面细胞极性基因的双基因变异》勘误。《分子遗传学与代谢》。2018年5月；124(1):94 - 100。doi:10.1016/j.ymgme.2018.03.005。2018年3月18日在线发表。https://pubmed.ncbi.nlm.nih.gov/29573971/ 。
Mol Genet Metab. 2021 Mar;132(3):211. doi: 10.1016/j.ymgme.2021.01.010. Epub 2021 Feb 10.
5
Corrigendum to "Nuclear Factor-Y is an adipogenic factor that regulates leptin gene expression"[Mol Metab 4 (2015) 392-405].勘误：“核因子-Y 是一种脂肪生成因子，可调节瘦素基因的表达”[Mol Metab 4 (2015) 392-405]。
Mol Metab. 2015 Jun 6;4(8):592. doi: 10.1016/j.molmet.2015.05.004. eCollection 2015 Aug.
6
Corrigendum to "A systematic cross-sectional survey of multiple sulfatase deficiency" [Mol Genet Metab. 2020 Aug;130(4):283-288].《多重硫酸酯酶缺乏症的系统横断面调查》的勘误 [《分子遗传学与代谢》。2020年8月；130(4):283 - 288]
Mol Genet Metab. 2020 Sep-Oct;131(1-2):284. doi: 10.1016/j.ymgme.2020.10.012. Epub 2020 Nov 2.
7
Corrigendum to "Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening" [Mol. Genet. Metab. 110 (2013) 218-221].《新生儿筛查检测出的蛋氨酸腺苷转移酶I/III缺乏症患者的临床和代谢发现》勘误 [《分子遗传学与代谢》110 (2013) 218 - 221]
Mol Genet Metab. 2015 Mar;114(3):486. doi: 10.1016/j.ymgme.2015.01.011. Epub 2015 Feb 11.
8
Corrigendum to "Pyridoxine-5'-phosphate oxidase (Pnpo) deficiency: Clinical and biochemical alterations associated with the C.347g>A (P.·Arg116gln) mutation" [Mol. Genet. Metab. 122/1-2 (2017) 135-142].
Mol Genet Metab. 2018 Dec;125(4):359. doi: 10.1016/j.ymgme.2018.02.017. Epub 2018 Mar 14.
9
Corrigendum to "GJC2 promoter mutations causing Pelizaeus-Merzbacher-like disease" [Mol. Genet. Metab. 111 (2014) 393-398].《“导致佩利措伊斯-梅茨巴赫样病的GJC2启动子突变”的勘误》[《分子遗传学与代谢》111(2014)393 - 398]
Mol Genet Metab. 2016 Nov;119(3):293. doi: 10.1016/j.ymgme.2016.06.011.
10
Corrigendum to "Aromatic amino acid decarboxylase deficiency: Molecular and metabolic basis and therapeutic outlook" [Mol Genet Metab. 2019 May;127(1):12-22].《芳香族氨基酸脱羧酶缺乏症：分子与代谢基础及治疗前景》的勘误[《分子遗传学与代谢》。2019年5月；127(1):12 - 22] 。
Mol Genet Metab. 2021 Sep-Oct;134(1-2):216. doi: 10.1016/j.ymgme.2021.06.010. Epub 2021 Jul 7.
Zotero 插件