Literature DB >> 35414925

Corrigendum.

.   

Abstract

[This corrects the article DOI: 10.1002/ccr3.4882.].
© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Entities:  

Year:  2022        PMID: 35414925      PMCID: PMC8978990          DOI: 10.1002/ccr3.5672

Source DB:  PubMed          Journal:  Clin Case Rep        ISSN: 2050-0904


In the article entitled “A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene,” which was previously published in Volume 9 Issue 12 of Clinical Case Reports, the statement regarding the shared first authorship was missed out in the original publication. Both Claire Balza and Giulia Garofalo share the first authorship for this article.
  1 in total

1.  A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene.

Authors:  Claire Balza; Giulia Garofalo; Teresa Cos; Julie Désir; Xin Kang; Kathelijn Keymolen; Julie Soblet; Kim Van Berkel; Catheline Vilain; Wafa Ben Abbou; Marie Cassart
Journal:  Clin Case Rep       Date:  2021-12-05
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.