Literature DB >> 30783265

Correction: Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort.

Qingping Zhang1, Xiaoxu Yang2, Jiaping Wang1, Jiarui Li2, Qixi Wu2, Yongxin Wen1, Ying Zhao1, Xiaoying Zhang1, He Yao3, Xiru Wu1, Shujie Yu4, Liping Wei5, Xinhua Bao6.   

Abstract

The second author Jiarui Li is now listed as a co-first author according to her contribution to this paper. The list of authors who contributed equally now reads: Qingping Zhang, Xiaoxu Yang, Jiaping Wang, and Jiarui Li. This has now been corrected in both the PDF and HTML versions of the Article.

Entities:  

Year:  2019        PMID： 30783265      PMCID： PMC7608369          DOI： 10.1038/s41436-019-0461-x

Source DB:  PubMed          Journal:  Genet Med        ISSN： 1098-3600            Impact factor:   8.822


Correction to: Genet Med advance online publication 8 November 2018; 10.1038/s41436-018-0348-2 The second author Jiarui Li is now listed as a co–first author according to her contribution to this paper. The list of authors who contributed equally now reads: Qingping Zhang, Xiaoxu Yang, Jiaping Wang, and Jiarui Li. This has now been corrected in both the PDF and HTML versions of the Article.
  2 in total

1.  A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndrome.

Authors:  Frenny Sheth; Harsh Sheth; Jhanvi Shah; Harsh Patel; Deepika Jain
Journal:  BMC Neurol       Date:  2021-12-02       Impact factor: 2.474

2.  A case of congenital Rett variant in a Chinese patient caused by a FOXG1 mutation.

Authors:  Yan Niu; Lirong Cao; Peng Zhao; Chunguan Cai
Journal:  Ann Saudi Med       Date:  2020-08-06       Impact factor: 1.526
  2 in total

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