Crossmark

Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype–phenotype correlation

Crossref DOI link: https://doi.org/10.1007/s10048-022-00699-0

Published Online: 2022-09-17

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Tábuas-Pereira, Miguel https://orcid.org/0000-0002-3988-614X
Guerreiro, Rita https://orcid.org/0000-0001-5879-3486
Kun-Rodrigues, Célia https://orcid.org/0000-0003-4528-0061
Almeida, Maria Rosário https://orcid.org/0000-0002-1889-5469
Brás, José https://orcid.org/0000-0001-8186-0333
Santana, Isabel https://orcid.org/0000-0002-8114-9434
Funding

Funding for this research was provided by:

National Institute on Aging (R01AG067426)
License Information

Text and Data Mining valid from 2022-09-17

Version of Record valid from 2022-09-17
More Information

Article History

Received: 2 July 2022

Accepted: 2 September 2022

First Online: 17 September 2022

Declarations

:

: The authors declare no competing interests.

Document is current

Any future updates will be listed below