(Q93550080)

English

Mutator phenotype of Werner syndrome is characterized by extensive deletions

correction to a scholarly article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

0 references

Mutator phenotype of Werner syndrome is characterized by extensive deletions (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

Werner syndrome

1 reference

based on heuristic

inferred from title

publication date

1 October 1989

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

October 1989

0 references

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

86

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

20

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

7994-7994

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

Identifiers

10.1073/PNAS.86.20.7994

0 references

1989PNAS...86.7994.

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC298199&resulttype=core&format=json

8 May 2020

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