A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in STUB1 and Exacerbated by TBP Repeat Expansions.

Reis MC, Patrun J, Ackl N, Winter P, Scheifele M, Danek A, Nolte D

Open source

DOI
10.3389/fnmol.2022.878236
Published
2022
Container
Frontiers in molecular neuroscience
Publisher
Not recorded
Open access
yes

Credibility signals

limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

Cite this work

BibTeX

@article{allodium:10.3389/fnmol.2022.878236,
  title = {A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in STUB1 and Exacerbated by TBP Repeat Expansions.},
  author = {Reis MC and Patrun J and Ackl N and Winter P and Scheifele M and Danek A and Nolte D},
  year = {2022},
  journal = {Frontiers in molecular neuroscience},
  doi = {10.3389/fnmol.2022.878236},
  url = {https://doi.org/10.3389/fnmol.2022.878236}
}

RIS

TY  - JOUR
TI  - A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in STUB1 and Exacerbated by TBP Repeat Expansions.
AU  - Reis MC
AU  - Patrun J
AU  - Ackl N
AU  - Winter P
AU  - Scheifele M
AU  - Danek A
AU  - Nolte D
PY  - 2022
JO  - Frontiers in molecular neuroscience
DO  - 10.3389/fnmol.2022.878236
UR  - https://doi.org/10.3389/fnmol.2022.878236
ER  - 

APA

MC, R., J, P., N, A., P, W., M, S., A, D., & D, N. (2022). A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in STUB1 and Exacerbated by TBP Repeat Expansions.. Frontiers in molecular neuroscience. https://doi.org/10.3389/fnmol.2022.878236

Source records