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Kortüm, F.* ; Kieninger, S.* ; Mazzola, P.* ; Kohl, S.* ; Wissinger, B.* ; Prokisch, H. ; Stingl, K.* ; Weisschuh, N.*

X-linked retinitis pigmentosa caused by non-canonical splice site variants in RPGR.

Int. J. Mol. Sci. 22:850 (2021)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
We aimed to validate the effect of non-canonical splice site variants in the RPGR gene in five patients from four families diagnosed with retinitis pigmentosa. Four variants located in intron 2 (c.154 + 3_154 + 6del), intron 3 (c.247 + 5G>A), intron 7 (c.779-5T>G), and intron 13 (c.1573-12A>G), respectively, were analyzed by means of in vitro splice assays. Splicing analysis revealed different aberrant splicing events, including exon skipping and intronic nucleotide addition, which are predicted to lead either to an in-frame deletion affecting relevant protein domains or to a frameshift of the open reading frame. Our data expand the landscape of pathogenic variants in RPGR, thereby increasing the genetic diagnostic rate in retinitis pigmentosa and allowing patients harboring the analyzed variants to be enrolled in clinical trials.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Rpgr ; X-linked ; In Vitro Splice Assay ; Non-canonical Splice Site Variant ; Retinitis Pigmentosa
Sprache englisch
Veröffentlichungsjahr 2021
HGF-Berichtsjahr 2021
ISSN (print) / ISBN 1661-6596
e-ISSN 1422-0067
Zeitschrift International Journal of Molecular Sciences
Quellenangaben Band: 22, Heft: 2, Seiten: , Artikelnummer: 850 Supplement: ,
Verlag MDPI
Verlagsort Basel
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Neurogenomics (ING)
POF Topic(s) 30205 - Bioengineering and Digital Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-503292-001
Förderungen Open Access Publishing Fund of the University of Tubingen
DOI 10.3390/ijms22020850
WOS ID WOS:000611889200001
Scopus ID 85099550958
PubMed ID 33467000
Erfassungsdatum 2021-03-30
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