Following the original article's publication [1] the authors asked for the correction of Fig. 2, since the names of the disease genes [GCH1 and PCBD1] in the figure published did not match the listed diseases [AR-GTPCHD and PCDD]. The correct Fig. 2 isshown below: In the context of the manuscript correction and inorder to match he text content, the words "apart from DHPRD" should be removed from the second row and second column of Table 4, as shown below: (Table Presented)
(The American Journal of Human Genetics 108, 186–193; January 7, 2021) In the originally published v...
The authors regret an error in the previously reported result concerning the nomenclature of a mutat...
Unfortunately, the original version of this article [1] contained an error. The figure titles for Fi...
An amendment to this paper has been published and can be accessed via the original article.Medicine,...
Abstract Following publication of the original article [1], the authors reported an error in Table 3...
(The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper or...
Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published onli...
correction de l'article hal-02620103International audienceThe original version of this article conta...
Following publication of the original article [1], we have been notified that Fig. 1 was published i...
The authors regret that the printed version of the above article contained an incomplete list of ref...
Correction During the production process for this article [1] some errors were introduced into Table...
The original paper of this article unfortunately contains error in the figure legend embedded in Fig...
During the preparation of this manuscript, the same sample was inadvertently included for the +/L100...
Unfortunately, the published article has errors in Table 1. In second case with MFN2 mutation the de...
Meerschaut I, Rochefort D, Revençu N, et al. FOXP1-related intellectual disability syndrome: a recog...
(The American Journal of Human Genetics 108, 186–193; January 7, 2021) In the originally published v...
The authors regret an error in the previously reported result concerning the nomenclature of a mutat...
Unfortunately, the original version of this article [1] contained an error. The figure titles for Fi...
An amendment to this paper has been published and can be accessed via the original article.Medicine,...
Abstract Following publication of the original article [1], the authors reported an error in Table 3...
(The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper or...
Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published onli...
correction de l'article hal-02620103International audienceThe original version of this article conta...
Following publication of the original article [1], we have been notified that Fig. 1 was published i...
The authors regret that the printed version of the above article contained an incomplete list of ref...
Correction During the production process for this article [1] some errors were introduced into Table...
The original paper of this article unfortunately contains error in the figure legend embedded in Fig...
During the preparation of this manuscript, the same sample was inadvertently included for the +/L100...
Unfortunately, the published article has errors in Table 1. In second case with MFN2 mutation the de...
Meerschaut I, Rochefort D, Revençu N, et al. FOXP1-related intellectual disability syndrome: a recog...
(The American Journal of Human Genetics 108, 186–193; January 7, 2021) In the originally published v...
The authors regret an error in the previously reported result concerning the nomenclature of a mutat...
Unfortunately, the original version of this article [1] contained an error. The figure titles for Fi...