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Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”

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Published in:Molecular Genetics & Genomic Medicine
Format: Online Article RSS Article
Published: 2026
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container_title Molecular Genetics & Genomic Medicine
description
discipline_display Genetics
discipline_facet Genetics
format Online Article
RSS Article
genre Journal Article
id rss_article:91828
institution FRELIP
journal_source_facet Molecular Genetics & Genomic Medicine
last_indexed 2026-06-16T02:03:04.397Z
publishDate 2026
publishDateSort 2026
record_format rss_article
spellingShingle Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”
Genetics
General
Genetics
sub_discipline_display General
sub_discipline_facet General
subject_display Genetics
General
Genetics
Genetics
General
Genetics
subject_facet Genetics
General
Genetics
title Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”
title_auth Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”
title_full Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”
title_fullStr Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”
title_full_unstemmed Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”
title_short Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”
title_sort correction to “identification and functional analysis of a novel nsd2 missense variant in a patient with rauch‐steindl syndrome”
topic Genetics
General
Genetics
url https://onlinelibrary.wiley.com/doi/10.1002/mgg3.70252?af=R