RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences

Detalles Bibliográficos
Autores principales: Gu, Hyunjung, Hong, Jinyoung, Lee, Woochang, Kim, Sung-Bae, Chun, Sail, Min, Won-Ki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Laboratory Medicine 2022
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677484/
https://www.ncbi.nlm.nih.gov/pubmed/34907111
http://dx.doi.org/10.3343/alm.2022.42.3.376
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author Gu, Hyunjung
Hong, Jinyoung
Lee, Woochang
Kim, Sung-Bae
Chun, Sail
Min, Won-Ki
author_facet Gu, Hyunjung
Hong, Jinyoung
Lee, Woochang
Kim, Sung-Bae
Chun, Sail
Min, Won-Ki
author_sort Gu, Hyunjung
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spelling pubmed-86774842022-05-01 RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences Gu, Hyunjung Hong, Jinyoung Lee, Woochang Kim, Sung-Bae Chun, Sail Min, Won-Ki Ann Lab Med Letter to the Editor Korean Society for Laboratory Medicine 2022-05-01 2022-05-01 /pmc/articles/PMC8677484/ /pubmed/34907111 http://dx.doi.org/10.3343/alm.2022.42.3.376 Text en © Korean Society for Laboratory Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Gu, Hyunjung
Hong, Jinyoung
Lee, Woochang
Kim, Sung-Bae
Chun, Sail
Min, Won-Ki
RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences
title RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences
title_full RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences
title_fullStr RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences
title_full_unstemmed RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences
title_short RNA Sequencing for Elucidating an Intronic Variant of Uncertain Significance (SDHD c.314+3A>T) in Splicing Site Consensus Sequences
title_sort rna sequencing for elucidating an intronic variant of uncertain significance (sdhd c.314+3a>t) in splicing site consensus sequences
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677484/
https://www.ncbi.nlm.nih.gov/pubmed/34907111
http://dx.doi.org/10.3343/alm.2022.42.3.376
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