Literature DB >> 29396438

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Jean-Louis Guéant1, Céline Chéry2, Abderrahim Oussalah2, Javad Nadaf3, David Coelho2, Thomas Josse2, Justine Flayac2, Aurélie Robert2, Isabelle Koscinski2, Isabelle Gastin2, Pierre Filhine-Tresarrieu2, Mihaela Pupavac3, Alison Brebner3, David Watkins3, Tomi Pastinen3, Alexandre Montpetit3, Fadi Hariri3, David Tregouët4, Benjamin A Raby5, Wendy K Chung6, Pierre-Emmanuel Morange7, D Sean Froese8, Matthias R Baumgartner8, Jean-François Benoist9, Can Ficicioglu10, Virginie Marchand11, Yuri Motorin11, Chrystèle Bonnemains2, François Feillet2, Jacek Majewski3, David S Rosenblatt3.   

Abstract

The original version of this Article contained an error in the title, which was incorrectly given as 'APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients'. This has now been corrected in both the PDF and HTML versions of the Article to read 'A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients'.

Entities:  

Year:  2018        PMID： 29396438      PMCID： PMC5797229          DOI： 10.1038/s41467-018-03054-w

Source DB:  PubMed          Journal:  Nat Commun        ISSN： 2041-1723            Impact factor:   14.919


Correction to: Nature Communications 10.1038/s41467-017-02306-5, published online 4 January 2018 The original version of this Article contained an error in the title, which was incorrectly given as “APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients”. This has now been corrected in both the PDF and HTML versions of the Article to read “A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients”.
  6 in total

1.  Screening for rare epigenetic variations in autism and schizophrenia.

Authors:  Paras Garg; Andrew J Sharp
Journal:  Hum Mutat       Date:  2019-03-21       Impact factor: 4.878

Review 2.  Epimutation in inherited metabolic disorders: the influence of aberrant transcription in adjacent genes.

Authors:  Jean-Louis Guéant; Youssef Siblini; Céline Chéry; Guillaume Schmitt; Rosa-Maria Guéant-Rodriguez; David Coelho; David Watkins; David S Rosenblatt; Abderrahim Oussalah
Journal:  Hum Genet       Date:  2022-02-21       Impact factor: 5.881

3.  A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.

Authors:  Paras Garg; Bharati Jadhav; Oscar L Rodriguez; Nihir Patel; Alejandro Martin-Trujillo; Miten Jain; Sofie Metsu; Hugh Olsen; Benedict Paten; Beate Ritz; R Frank Kooy; Jozef Gecz; Andrew J Sharp
Journal:  Am J Hum Genet       Date:  2020-09-15       Impact factor: 11.025

4.  Effects of Chinese wolfberry and Astragalus extract on the antioxidant capacity of Tibetan pig liver.

Authors:  Zhuang Hao; Zhen Li; Jinjin Huo; Jiandong Li; Fenghua Liu; Peng Yin
Journal:  PLoS One       Date:  2021-01-27       Impact factor: 3.240

5.  Acute Lymphoblastic Leukemia in Combined Methylmalonic Acidemia and Homocysteinemia (cblC Type): A Case Report and Literature Review.

Authors:  Jun Zhu; Shuisen Wan; Xueqi Zhao; Binlu Zhu; Yuan Lv; Hongkun Jiang
Journal:  Front Genet       Date:  2022-04-14       Impact factor: 4.772

6.  Multiple sclerosis and intracellular cobalamin defect (MMACHC/PRDX1) comorbidity in a young male.

Authors:  Luca Pollini; Manuela Tolve; Francesca Nardecchia; Serena Galosi; Claudia Carducci; Emanuele di Carlo; Carla Carducci; Vincenzo Leuzzi
Journal:  Mol Genet Metab Rep       Date:  2020-01-07
  6 in total

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