Additional file 1: Figure S2. of HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report

Sequencing results of the patient and his parents with reverse primer. As the HDR mutation observed in the affected child was not present in any of the parents, they represent de novo mutations. (TIFF 1424Â kb)

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PID https://www.doi.org/10.6084/m9.figshare.c.3914992_d1.v1
URL https://dx.doi.org/10.6084/m9.figshare.c.3914992_d1.v1
URL http://dx.doi.org/10.6084/m9.figshare.c.3914992_d1.v1
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Author Yang, Aram
Author Jinsup Kim
Author Chang-Seok Ki
Author Hong, Sung
Author Cho, Sung, 0000-0003-2913-059X
Author Jin, Dong-Kyu
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Collected From Datacite; figshare
Hosted By figshare
Publication Date 2017-10-27
Publisher Figshare
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Language UNKNOWN
Resource Type Dataset; Image
keyword FOS: Biological sciences
system:type dataset
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Source https://science-innovation-policy.openaire.eu/search/dataset?datasetId=dedup_wf_001::4e936a6812231fded4ceb4a957c600b7
Author jsonws_user
Version None
Last Updated 14 January 2021, 14:26 (CET)
Created 14 January 2021, 14:26 (CET)